Class II · Moderate risk Terminated
Diclofenac Sodium and Misoprostol Delayed-Release Tablets, 75mg/0.2mg, Rx only, Manufactured by Watson Laboratories, Inc…
Reason Failed Tablet/Capsule Specifications: Broken tablets
Is Diclofenac recalled?
29 FDA recalls mention Diclofenac. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Diclofenac.
Class III · Low risk Terminated
Voltaren Gel (diclofenac sodium topical gel) 1%, for topical use only, RX only, a) Packaged in 20 gm tubes, NDC 63481-684-83…
Reason Labeling: Incorrect or Missing Lot and/or Expiration date; The Lot and/or Expiration date on the tube may not be legible in this lot.
Class II · Moderate risk Terminated
DICLOFENAC SODIUM, SDPF - (0.1ML SYRINGE, 30G, 1/2") 500MCG/0.1ML INJECTABLE 0.5 ML, 2 ML, 4 ML (3 DIFFERENT PRODUCTS)
Reason Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all Sterile Human Drugs distributed between 11/21/2011 and 05/21/2012 because…
Class II · Moderate risk Terminated
Arthrotec 75 (diclofenac sodium and misoprostol) tablets, 75 mg/200 mcg, a) 30-count tablets per bottle (NDC 54868-4165-1); b)…
Reason Tablet Separation: The manufacturer of Arthrotec had recalled the lots that were used to re-package this product because they may contain broken…
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