Recalls of common over-the-counter and prescription pain relievers.
415 recalls in this category, newest first.
Reason Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.
Reason Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.
Reason Labeling: Label Mix-Up: A complaint from a pharmacist was received that the entire contents of 1 bottle labeled as Rugby label Enteric Coated Aspirin…
Reason Defective container: products are packaged in pouches which may not have been fully sealed
Reason Defective container: products are packaged in pouches which may not have been fully sealed
Reason Defective container: products are packaged in pouches which may not have been fully sealed
Reason Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
Reason Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
Reason Failed Impurities/Degradation:Specifications:Unknown degradant found during stability testing
Reason Failed Impurities/Degradation:Specifications:Unknown degradant found during stability testing.
Reason Failed Impurities/Degradation:Specifications:Unknown degradant found during stability testing
Reason Failed Impurities/Degradation:Specifications:Unknown degradant found during stability testing.
Reason Failed Impurities/Degradation:Specifications:Unknown degradant found during stability testing.
Reason Failed Impurities/Degradation:Specifications:Unknown degradant found during stability testing.
Reason Failed Impurities/Degradation:Specifications:Unknown degradant found during stability testing.
Reason Labeling: Not Elsewhere Classified: Pentrexcilina Tablets and Pentrexcilina Liquid are being recalled because the product labels are misleading…
Reason Chemical Contamination: Gabapentin Sodium tablets is recalled due to complaints related to an off - odor described as moldy, musty or fishy in nature.
Reason Failed Tablet/Capsule Specifications: Broken tablets
Reason Failed Tablet/Capsule Specifications: Broken tablets
Reason Labeling: Not Elsewhere Classified: This unit dose product is being recalled because the product's name includes the word "Children's" which is…
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.
Reason Subpotent; 12 month time point for the active ingredient Phenylephrine HCl.
Reason Superpotent (Multiple Ingredient) Drug: Oversized tablets resulting in superpotent assays of both the hydrocodone and acetaminophen components.
Reason Superpotent (Multiple Ingredient) Drug: Complaint received of oversized tablets.
Reason Adulterated Presence of Foreign Tablets: A customer complaint was received that a bottle of Tramadol HCl Tablets USP 50 mg contained some tablets of…
Tell us which medications you take. If the FDA recalls one, we email you - in plain English, with what to do. Free.