{"id":849,"date":"2017-07-28T11:56:44","date_gmt":"2017-07-28T10:56:44","guid":{"rendered":"https:\/\/www.groupactionlawyers.co.uk\/blog\/?p=849"},"modified":"2017-07-28T12:04:42","modified_gmt":"2017-07-28T11:04:42","slug":"diclo-sr-75-pain-relief-tablets-class-2-recall","status":"publish","type":"post","link":"https:\/\/www.groupactionlawyers.co.uk\/blog\/diclo-sr-75-pain-relief-tablets-class-2-recall","title":{"rendered":"Class 2 recall for Diclo-SR 75 pain-relief tablets"},"content":{"rendered":"<p>A Watford-based pharmaceutical company has issued a voluntary recall for batches of <em>Diclo-SR 75<\/em> pain relief tablets &#8211; AKA diclofenac sodium.<\/p>\n<p>The tablets are commonly used for pain relief and swelling for arthritis, musculoskeletal disorders, gout and pain caused by injury or minor surgery. The tablets are classified in a group of medicines called non-steroidal anti-inflammatory drugs.<br \/>\n<!--more--><\/p>\n<h2>Side-effects<\/h2>\n<p>Medicines commonly have side-effects, and the risk can be greater with higher doses and prolonged use of the medication.<\/p>\n<p>Strides Pharma U.K. Ltd (trading as Co-pharma) may have exacerbated the panic for some users, noting some batches of the medicines showed some high trending stability results in impurity tests.<\/p>\n<h3>Affected batches<\/h3>\n<p>The affected batches are reportedly as follows:<\/p>\n<div class=\"table-responsive\">\n<table class=\"table table-striped\">\n<theader>\n<tr>\n<th>Batch Number<\/th>\n<th>Expiry Date<\/th>\n<th>Pack Size<\/th>\n<th>First Distributed<\/th>\n<\/tr>\n<\/theader>\n<tbody>\n<tr>\n<td>7226423<\/td>\n<td>02.2019<\/td>\n<td>28 tablets<\/td>\n<td>07\/08\/2016<\/td>\n<\/tr>\n<tr>\n<td>7226424<\/td>\n<td>02.2019<\/td>\n<td>28 tablets<\/td>\n<td>07\/08\/2016<\/td>\n<\/tr>\n<tr>\n<td>7226425<\/td>\n<td>03.2019<\/td>\n<td>28 tablets<\/td>\n<td>07\/08\/2106<\/td>\n<\/tr>\n<tr>\n<td>7227697<\/td>\n<td>06.2019<\/td>\n<td>56 tablets<\/td>\n<td>20\/10\/2016<\/td>\n<\/tr>\n<tr>\n<td>7227698<\/td>\n<td>06.2019<\/td>\n<td>56 tablets<\/td>\n<td>20\/10\/2016<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/div>\n<h3>Recall classes<\/h3>\n<p>Medicine recalls are often based on a tiered structure:<\/p>\n<div class=\"well\">\n<ul>\n<li>Class 1: requires immediate recall because the product poses a serious or life-threatening risk to health.<\/li>\n<li>Class 2: specifies a recall within 48 hours because the defect could harm the patient, but isn&#8217;t life threatening.<\/li>\n<li>Class 3: requires action to be taken within five days because the defect is unlikely to harm patients and is being carried out for reasons other than patient safety.<\/li>\n<li>Class 4: advises caution to be exercised when using the product but indicates the product poses no threat to patient safety.<\/li>\n<\/ul>\n<\/div>\n<h3>Class 2 recall initiated<\/h3>\n<p>The UK&#8217;s Medicines and Healthcare products Regulatory (MHRA) has issued this as a Class 2 recall.<\/p>\n<p>Generally, Medical Alerts are graded according to the seriousness of the threat to the patient&#8217;s health, with grading from class 1 to class 4. The current Alert has been classified under a &#8216;class 2 medicines recall&#8217;. A class 2 specifies that the recall should be made within 48 hours.<\/p>\n<h3>MHRA and EMA<\/h3>\n<p>The MHRA&#8217;s role is critical for consumer safety and ensures patients are duly informed of safety risks. Should there be an issue with medicines and medical equipment, the MHRA has the authority to take the product\/equipment off of the market, announce a recall and to halt all production until the problem is rectified.<\/p>\n<p>The MHRA also works in conjunction with the European Medicines Agency (EMA) who are tasked with the responsibility of supervision for medicines across Europe.<\/p>\n<h3>Alerts to be circulated<\/h3>\n<p>A Drug Alert has yet to be circulated in the healthcare community. The MHRA has asked for the Drug Alert to be brought to the attention of any &#8216;relevant contacts&#8217; with a copy of the drug alert letter. NHS Regional Teams have been asked to forward the Alert onto community pharmacists, relevant clinics and dispensing GPs for action.<\/p>\n<p>The class recall for the Diclo-SR tablets is listed quite highly. Although the definition of class 2 recalls state that it isn&#8217;t life threatening, it doesn&#8217;t give the assurances that it wouldn&#8217;t cause injuries through continued use.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>A Watford-based pharmaceutical company has issued a voluntary recall for batches of Diclo-SR 75 pain relief tablets &#8211; AKA diclofenac sodium. The tablets are commonly used for pain relief and swelling for arthritis, musculoskeletal disorders, gout and pain caused by injury or minor surgery. The tablets are classified in a group of medicines called non-steroidal &hellip; <a href=\"https:\/\/www.groupactionlawyers.co.uk\/blog\/diclo-sr-75-pain-relief-tablets-class-2-recall\" class=\"more-link\">Continue reading <span class=\"screen-reader-text\">Class 2 recall for Diclo-SR 75 pain-relief tablets<\/span><\/a><\/p>\n","protected":false},"author":2,"featured_media":853,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_jetpack_newsletter_access":"","_jetpack_dont_email_post_to_subs":false,"_jetpack_newsletter_tier_id":0,"_jetpack_memberships_contains_paywalled_content":false,"_jetpack_memberships_contains_paid_content":false,"footnotes":"","jetpack_publicize_message":"","jetpack_publicize_feature_enabled":true,"jetpack_social_post_already_shared":true,"jetpack_social_options":{"image_generator_settings":{"template":"highway","default_image_id":0,"font":"","enabled":false},"version":2},"jetpack_post_was_ever_published":false},"categories":[5],"tags":[8],"class_list":["post-849","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-medical","tag-recalls"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.5 - 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It's an active 'serotonin-norepinephrine reuptake inhibitor', providing pain relief for patients with diabetes or sufferers from chronic or widespread pain. The drug is commonly prescribed to people with arthritis\u2026","rel":"","context":"In &quot;Latest&quot;","block_context":{"text":"Latest","link":"https:\/\/www.groupactionlawyers.co.uk\/blog\/category\/latest"},"img":{"alt_text":"drugs","src":"https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/11\/drugs-recall-750x250.png?fit=750%2C250&ssl=1&resize=350%2C200","width":350,"height":200,"srcset":"https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/11\/drugs-recall-750x250.png?fit=750%2C250&ssl=1&resize=350%2C200 1x, https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/11\/drugs-recall-750x250.png?fit=750%2C250&ssl=1&resize=525%2C300 1.5x, https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/11\/drugs-recall-750x250.png?fit=750%2C250&ssl=1&resize=700%2C400 2x"},"classes":[]},{"id":620,"url":"https:\/\/www.groupactionlawyers.co.uk\/blog\/does-small-crack-blistering-tablet-packaging-impact-their-effectiveness","url_meta":{"origin":849,"position":1},"title":"Class 3 recall: does the small crack in the blistering of tablet packaging impact their effectiveness?","author":"Admin","date":"19th April 2017","format":false,"excerpt":"The Medicines and Healthcare products Regulatory Agency (MHRA) has recommended recalling instant pain relief tablets due to an issue with some batches. Bayer plc is a pharmaceutical company who manufactured the pain relief tablets in question; Alka-Seltzer Original & Alka-Seltzer XS. Bayer noticed an issue with the blister foil and\u2026","rel":"","context":"In &quot;Medical&quot;","block_context":{"text":"Medical","link":"https:\/\/www.groupactionlawyers.co.uk\/blog\/category\/medical"},"img":{"alt_text":"drugs","src":"https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/11\/drugs-recall-750x250.png?fit=750%2C250&ssl=1&resize=350%2C200","width":350,"height":200,"srcset":"https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/11\/drugs-recall-750x250.png?fit=750%2C250&ssl=1&resize=350%2C200 1x, https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/11\/drugs-recall-750x250.png?fit=750%2C250&ssl=1&resize=525%2C300 1.5x, https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/11\/drugs-recall-750x250.png?fit=750%2C250&ssl=1&resize=700%2C400 2x"},"classes":[]},{"id":406,"url":"https:\/\/www.groupactionlawyers.co.uk\/blog\/chewy-calcium-vitamin-d-tablets-being-recalled-for-impurities","url_meta":{"origin":849,"position":2},"title":"Chewy calcium and vitamin-D tablets are being recalled for impurities","author":"Admin","date":"28th December 2016","format":false,"excerpt":"Teva U.K. Limited - a global pharmaceutical company - has recalled a batch of class 2 medicines due to a possible metal contamination. The pharmaceutical company has recently made a precautionary batch recall for a 'small number' of Evacal D3 chewable tablets. The tablets are a calcium-vitamin D supplement used\u2026","rel":"","context":"In &quot;Medical&quot;","block_context":{"text":"Medical","link":"https:\/\/www.groupactionlawyers.co.uk\/blog\/category\/medical"},"img":{"alt_text":"drugs","src":"https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/11\/drugs-recall-750x250.png?fit=750%2C250&ssl=1&resize=350%2C200","width":350,"height":200,"srcset":"https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/11\/drugs-recall-750x250.png?fit=750%2C250&ssl=1&resize=350%2C200 1x, https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/11\/drugs-recall-750x250.png?fit=750%2C250&ssl=1&resize=525%2C300 1.5x, https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/11\/drugs-recall-750x250.png?fit=750%2C250&ssl=1&resize=700%2C400 2x"},"classes":[]},{"id":2628,"url":"https:\/\/www.groupactionlawyers.co.uk\/blog\/sabril-tablets-and-granules-concerns-raised","url_meta":{"origin":849,"position":3},"title":"Sabril Tablets and Granules Concerns Raised","author":"Author","date":"10th October 2023","format":false,"excerpt":"Potential concerns that have arisen regarding the potential safety of Sabril tablets and granules have been publicised by UK health regulators. The medications, manufactured by Aventis Pharma Limited (a subsidiary of Sanofi), have reportedly been subject to advice issued by The Medicines and Healthcare products Regulatory Agency (MHRA). The regulator\u2026","rel":"","context":"In &quot;Group Actions&quot;","block_context":{"text":"Group Actions","link":"https:\/\/www.groupactionlawyers.co.uk\/blog\/category\/group-actions"},"img":{"alt_text":"Sabril tablets and granules","src":"https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/A-USED-DLL-GAL-GF-SI-MED-serious_injury-4.jpg?fit=1000%2C667&ssl=1&resize=350%2C200","width":350,"height":200,"srcset":"https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/A-USED-DLL-GAL-GF-SI-MED-serious_injury-4.jpg?fit=1000%2C667&ssl=1&resize=350%2C200 1x, https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/A-USED-DLL-GAL-GF-SI-MED-serious_injury-4.jpg?fit=1000%2C667&ssl=1&resize=525%2C300 1.5x, https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/A-USED-DLL-GAL-GF-SI-MED-serious_injury-4.jpg?fit=1000%2C667&ssl=1&resize=700%2C400 2x"},"classes":[]},{"id":770,"url":"https:\/\/www.groupactionlawyers.co.uk\/blog\/sodium-cromoglicate-eye-drops-mhra-class-2-medicines-recall","url_meta":{"origin":849,"position":4},"title":"MHRA publishes a class 2 Medicines recall for Sodium Cromoglicate eye drops","author":"Admin","date":"28th June 2017","format":false,"excerpt":"The Medicines and Health products Regulation Agency (MHRA) published a medical drug alert on the 18th May 2017 issuing a precautionary recall for bottles of eye drops amidst concerns that the solution can solidify in its container. Sodium Cromoglicate solution eye drops are typically used to treat red, watery and\u2026","rel":"","context":"In &quot;Medical&quot;","block_context":{"text":"Medical","link":"https:\/\/www.groupactionlawyers.co.uk\/blog\/category\/medical"},"img":{"alt_text":"eye compensation","src":"https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/eye-drops-recall-min.png?fit=725%2C250&ssl=1&resize=350%2C200","width":350,"height":200,"srcset":"https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/eye-drops-recall-min.png?fit=725%2C250&ssl=1&resize=350%2C200 1x, https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/eye-drops-recall-min.png?fit=725%2C250&ssl=1&resize=525%2C300 1.5x, https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/eye-drops-recall-min.png?fit=725%2C250&ssl=1&resize=700%2C400 2x"},"classes":[]},{"id":517,"url":"https:\/\/www.groupactionlawyers.co.uk\/blog\/arthritis-tablets-may-adversely-affect-braille-users","url_meta":{"origin":849,"position":5},"title":"Arthritis tablets may adversely affect users who rely solely on Braille","author":"Admin","date":"6th February 2017","format":false,"excerpt":"The Medicines and Healthcare products Regulatory Agency (MHRA) recently issued a caution relating to a drug that treats adult patients with active rheumatoid arthritis or active psoriatic arthritis. Global pharmaceutical company\u00a0Sanofi informed the medical agency of the error on the Braille on the packaging of some batches of the Arava\u2026","rel":"","context":"In &quot;Medical&quot;","block_context":{"text":"Medical","link":"https:\/\/www.groupactionlawyers.co.uk\/blog\/category\/medical"},"img":{"alt_text":"","src":"https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/11\/xarelto-concerns.png?fit=725%2C250&ssl=1&resize=350%2C200","width":350,"height":200,"srcset":"https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/11\/xarelto-concerns.png?fit=725%2C250&ssl=1&resize=350%2C200 1x, https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/11\/xarelto-concerns.png?fit=725%2C250&ssl=1&resize=525%2C300 1.5x, https:\/\/i0.wp.com\/www.groupactionlawyers.co.uk\/blog\/wp-content\/uploads\/2016\/11\/xarelto-concerns.png?fit=725%2C250&ssl=1&resize=700%2C400 2x"},"classes":[]}],"jetpack_sharing_enabled":true,"_links":{"self":[{"href":"https:\/\/www.groupactionlawyers.co.uk\/blog\/wp-json\/wp\/v2\/posts\/849","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.groupactionlawyers.co.uk\/blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.groupactionlawyers.co.uk\/blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.groupactionlawyers.co.uk\/blog\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/www.groupactionlawyers.co.uk\/blog\/wp-json\/wp\/v2\/comments?post=849"}],"version-history":[{"count":4,"href":"https:\/\/www.groupactionlawyers.co.uk\/blog\/wp-json\/wp\/v2\/posts\/849\/revisions"}],"predecessor-version":[{"id":855,"href":"https:\/\/www.groupactionlawyers.co.uk\/blog\/wp-json\/wp\/v2\/posts\/849\/revisions\/855"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.groupactionlawyers.co.uk\/blog\/wp-json\/wp\/v2\/media\/853"}],"wp:attachment":[{"href":"https:\/\/www.groupactionlawyers.co.uk\/blog\/wp-json\/wp\/v2\/media?parent=849"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.groupactionlawyers.co.uk\/blog\/wp-json\/wp\/v2\/categories?post=849"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.groupactionlawyers.co.uk\/blog\/wp-json\/wp\/v2\/tags?post=849"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}