Medicines, 2014
Shortlist up to four to read them side by side.
1,562 medicine recalls FDA’s Enforcement Report published in 2014, newest first; 18,075 in all since 2012.
FDA’s medicine recalls, as its Enforcement Report classifies them, from June 2012. Lists of FDA’s records can’t be saved for alerts: openFDA asks that its data not be used to alert the public (openFDA); FDA’s own emails do that. Copied Nov 5, 2026.
1,562of 1,562 medicine recallsshown with your filters
The list
- Medicine recall Laroscorbine Platinium (vitamin C/collagen) injectable I.V Marketed Without An Approved NDA/ANDA: Product is sold over the counter whose labeling includes drug claims to act as an antidote. Class IIFDA’s classMay 21, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 21, 2014ClassClass IIStatusCompletedWhereNationwide
- Medicine recall Tatiomax (reduced glutathione/hydrolyzed collagen) powder for injection vials, 1200 mg/200 mg, 10-count vials… Marketed Without An Approved NDA/ANDA: Product is sold over the counter whose labeling includes drug claims to act as an antidote. Class IIFDA’s classMay 21, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 21, 2014ClassClass IIStatusCompletedWhereNationwide
- Medicine recall Saluta (reduced glutathione) Powder for Injection, 600 mg/vial Marketed Without An Approved NDA/ANDA: Parenteral product is labeled for use as an antidote. Class IIFDA’s classMay 21, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 21, 2014ClassClass IIStatusCompletedWhereNationwide
- Medicine recall Relumins Advanced Glutathione (lyophilized glutathione/vitamin C) injectable solution, 1500 mg/500 mg Marketed Without An Approved NDA/ANDA: Product is sold over the counter whose labeling indicates it is to be used parenterally for drug claims. Class IIFDA’s classMay 21, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 21, 2014ClassClass IIStatusCompletedWhereNationwide
- Medicine recall Vitamin C (ascorbic acid) Injection, USP, 500 mg per 2 mL, 50 x 2 mL ampoules per box Marketed Without An Approved NDA/ANDA: Parenteral product is sold over the counter whose labeling indicates it is to be used for the treatment of disease. Class IIFDA’s classMay 21, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 21, 2014ClassClass IIStatusCompletedWhereNationwide
- Medicine recall Sterile Water for Injection, 5 mL ampoules Marketed Without An Approved NDA/ANDA: Product is sold over the counter whose labeling indicates it is to be used for parenteral injection. Class IIFDA’s classMay 21, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 21, 2014ClassClass IIStatusCompletedWhereNationwide
- Medicine recall REUMOFAN PLUS Tablets, 30 Tablet Bottles, OTC Marketed Without an Approved NDA/ANDA; Product contains undeclared diclofenac and methocarbamol. FDA Class I, its most serious class Class IFDA’s class (needs attention)May 21, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMay 21, 2014ClassClass IStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall Smart Tab First Aid ezRefill System Ibuprofen dispenser boxes (Item Number FAE 7014), 20 count boxes, First… First Aid Only, Inc is recalling Smart Tab First Aid ezRefill System Ibuprofen boxes and First Aid Cabinets containing these Ibuprofen boxes. Class IIFDA’s classMay 21, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 21, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall METHYLDOPA Tablets USP, 500 mg, 100 count bottle CGMP Deviations; laboratory testing was not followed in accordance with GMP requirements Class IIFDA’s classMay 21, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 21, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Metoprolol Succinate Extended-Release Tablets, USP, 50 mg, 30-count bottle Failed Dissolution Specifications: failure of dissolution test observed at nine month time point. Class IIFDA’s classMay 14, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 14, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Metformin Hydrochloride Tablets USP 500 mg, 500 tablets Defective container: Product distributed without inner seal on bottles. Class IIFDA’s classMay 14, 2014in FDA’s Enforcement Report4 statesnamed in where it went PublishedMay 14, 2014ClassClass IIStatusTerminatedWhereConnecticut, Illinois, New Jersey and Utah
- Medicine recall Metformin Hydrochloride Tablets USP 1000 mg, 500 tablets Defective container: Product distributed without inner seal on bottles. Class IIFDA’s classMay 14, 2014in FDA’s Enforcement Report4 statesnamed in where it went PublishedMay 14, 2014ClassClass IIStatusTerminatedWhereConnecticut, Illinois, New Jersey and Utah
- Medicine recall Mangiacotti - Lemon Verbena Hand Sanitizer Spray, alcohol free, 0.5 fl Microbial Contamination of Non-Sterile Products: Elevated counts of bacteria was found, Serratia liquefaciens. Class IIFDA’s classMay 14, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 14, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Mangiacotti - Lavender Hand Sanitizer Spray, alcohol free, 0.5 fl Oz. 15 mL spray bottle Microbial Contamination of Non-Sterile Products: Elevated counts of bacteria was found, Serratia liquefaciens. Class IIFDA’s classMay 14, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 14, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Mangiacotti - Ocean Hand Sanitizer Spray, alcohol free, 0.5 fl Oz. 15 mL spray bottle Microbial Contamination of Non-Sterile Products: Elevated counts of bacteria was found, Serratia liquefaciens. Class IIFDA’s classMay 14, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 14, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Mangiacotti - Clementine Hand Sanitizer Spray, alcohol free, 0.5 fl Oz. 15 mL spray bottle Microbial Contamination of Non-Sterile Products: Elevated counts of bacteria was found, Serratia liquefaciens. Class IIFDA’s classMay 14, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 14, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Mangiacotti - Pomegranate Hand Sanitizer Spray, alcohol free, 0.5 fl Oz. 15 mL spray bottle Microbial Contamination of Non-Sterile Products: Elevated counts of bacteria was found, Serratia liquefaciens. Class IIFDA’s classMay 14, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 14, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Mangiacotti - Ginger Lime Hand Sanitizer Spray, alcohol free, 0.5 fl Oz. 15 mL spray bottle Microbial Contamination of Non-Sterile Products: Elevated counts of bacteria was found, Serratia liquefaciens. Class IIFDA’s classMay 14, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 14, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Liptruzet (ezetimibe and atorvastin) tablets,10 mg/10 mg, a) 30 count blister (NDC 66582-320-30), b) 90 count… This recall of LIPTRUZET is being initiated due to packaging defects. Class IIIFDA’s classMay 14, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMay 14, 2014ClassClass IIIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall Liptruzet (ezetimibe and atorvastin) tablets,10 mg/20 mg, a) 30 count blister (NDC 66582-321-30), b) 90 count… This recall of LIPTRUZET is being initiated due to packaging defects. Class IIIFDA’s classMay 14, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMay 14, 2014ClassClass IIIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall Liptruzet (ezetimibe and atorvastin) tablets,10 mg/40 mg, a) 30 count blister (NDC 66582-322-30), b) 90 count… This recall of LIPTRUZET is being initiated due to packaging defects. Class IIIFDA’s classMay 14, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMay 14, 2014ClassClass IIIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall Liptruzet (ezetimibe and atorvastin) tablets,10 mg/80 mg, a) 30 count blister (NDC 66582-323-30), b) 90 count… Defective Container; some of the outer laminate foil pouches allowed in air and moisture, which could potentially decrease the effectiveness or change the… Class IIIFDA’s classMay 14, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMay 14, 2014ClassClass IIIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall Azathioprine Tablets USP, 50 mg, 100 count bottle Labeling: Incorrect or Missing Lot and/or Exp Date: This recall is being conducted because the product was given 36 month expiration dates instead of the filed… Class IIIFDA’s classMay 14, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 14, 2014ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Mercaptopurine Tablets USP, 50 mg, 25 count bottle Labeling: Incorrect or Missing Lot and/or Exp Date: This recall is being conducted because the product was given 36 month expiration dates instead of the filed… Class IIIFDA’s classMay 14, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 14, 2014ClassClass IIIStatusTerminatedWhereNationwide
- Medicine recall Phosphatidylcholine Solution for Injection, 50 mg/ mL, 50 mL Vial Labeling: Incorrect Expiration Date; Expiration date is earlier than listed on vial. Class IIFDA’s classMay 7, 2014in FDA’s Enforcement Report4 statesnamed in where it went PublishedMay 7, 2014ClassClass IIStatusTerminatedWhereMissouri, Mississippi, Tennessee and Wisconsin
- Medicine recall Papaverine 60 mg, Phentolamine 4 mg, and Atropine 0.3 mg Solution, 10 mL Vial Labeling: Incorrect Expiration Date; Expiration date is earlier than listed on vial. Class IIIFDA’s classMay 7, 2014in FDA’s Enforcement Report4 statesnamed in where it went PublishedMay 7, 2014ClassClass IIIStatusTerminatedWhereMissouri, Mississippi, Tennessee and Wisconsin
- Medicine recall Polidocanol 1% Solution, 50 mL Vial Labeling: Incorrect Expiration Date; Expiration date is earlier than listed on vial. Class IIIFDA’s classMay 7, 2014in FDA’s Enforcement Report4 statesnamed in where it went PublishedMay 7, 2014ClassClass IIIStatusTerminatedWhereMissouri, Mississippi, Tennessee and Wisconsin
- Medicine recall Polidocanol 3% Solution, 50 mL Vial Presence of Particulate Matter Class IIFDA’s classMay 7, 2014in FDA’s Enforcement Report4 statesnamed in where it went PublishedMay 7, 2014ClassClass IIStatusTerminatedWhereMissouri, Mississippi, Tennessee and Wisconsin
- Medicine recall Sevoflurane, USP (Inhalation Anesthetic) Failed pH Specifications: product was too acidic. Class IIFDA’s classMay 7, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 7, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Human Chorionic Gonadotropin, EP (HCG) Labeling: Label Error on Declared Strength; Firm states that erroneous potency information was found on the label. FDA Class I, its most serious class Class IFDA’s class (needs attention)May 7, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 7, 2014ClassClass IStatusTerminatedWhereNationwide
- Medicine recall Cefoxitin for Injection and Dextrose Injection, 1 g in Duplex, 50 mL Container Presence of Particulate Matter: B. FDA Class I, its most serious class Class IFDA’s class (needs attention)May 7, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMay 7, 2014ClassClass IStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall 0.9 % Sodium Chloride Injection USP in PAB 50 mL partial fill Presence of Particulate Matter: B. FDA Class I, its most serious class Class IFDA’s class (needs attention)May 7, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMay 7, 2014ClassClass IStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall Ceftriaxone for Injection and Dextrose Injection, 1 g in Duplex, 50 mL Container Presence of Particulate Matter: B. FDA Class I, its most serious class Class IFDA’s class (needs attention)May 7, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMay 7, 2014ClassClass IStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall Cefepime for Injections USP and Dextrose Injection USP, 1 g in Duplex, 50 mL Container Presence of Particulate Matter: B. FDA Class I, its most serious class Class IFDA’s class (needs attention)May 7, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMay 7, 2014ClassClass IStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall Cefazolin for Injection USP and Dextrose Injections USP, 1 g in Duplex, 50 mL Container Presence of Particulate Matter: B. FDA Class I, its most serious class Class IFDA’s class (needs attention)May 7, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMay 7, 2014ClassClass IStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall Cefazolin for Injection USP and Dextrose Injection USP, 2 g in Duplex, 50 mL Container Presence of Particulate Matter: B. FDA Class I, its most serious class Class IFDA’s class (needs attention)May 7, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMay 7, 2014ClassClass IStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall 0.9 % Sodium Chloride Injection USP, 1000 mL Presence of Particulate Matter: B. FDA Class I, its most serious class Class IFDA’s class (needs attention)May 7, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMay 7, 2014ClassClass IStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall 6.9% FreAmine HBC (Amino Acid Injection), partial fill container 750 mL in a 1000 mL container Presence of Particulate Matter: B. FDA Class I, its most serious class Class IFDA’s class (needs attention)May 7, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMay 7, 2014ClassClass IStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall 15% Amino Acids Injection PBP Glass, 1000 mL Presence of Particulate Matter: B. FDA Class I, its most serious class Class IFDA’s class (needs attention)May 7, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMay 7, 2014ClassClass IStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall TrophAmine (10% Amino Acid Injection), 500 mL Container, Rx Only, Catalog No. S9341-SS, Sterile, Single Dose… Presence of Particulate Matter: B. FDA Class I, its most serious class Class IFDA’s class (needs attention)May 7, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMay 7, 2014ClassClass IStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall ProcalAmine (3% Amino Acid and 3% Glycerin Injection with Electrolytes) 1000 mL Container, Rx Only, Catalog… Presence of Particulate Matter: B. FDA Class I, its most serious class Class IFDA’s class (needs attention)May 7, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMay 7, 2014ClassClass IStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall Hyperlyte CR (Multi-Electrolyte Concentrate), 20 mL/dose, 250 mL Container Presence of Particulate Matter: B. FDA Class I, its most serious class Class IFDA’s class (needs attention)May 7, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMay 7, 2014ClassClass IStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall Dianeal PD-2 Peritoneal Dialysis Solution with 1.5% Dextrose, 6000 mL Ambu-Flex II container Non-Sterility: Complaints of leaks and particulate matter identified as mold in the solution bag and the overpouch. FDA Class I, its most serious class Class IFDA’s class (needs attention)May 7, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 7, 2014ClassClass IStatusTerminatedWhereNationwide
- Medicine recall Adipotrim XT, New Powerful Formula, 30 rapid release capsules per bottle, Dietary Supplement,… Marketed Without an Approved NDA/ANDA: FDA lab results found undeclared API Fluoxetine in this dietary supplement. FDA Class I, its most serious class Class IFDA’s class (needs attention)May 7, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMay 7, 2014ClassClass IStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall Lidocaine HCl Injection, USP, 2%, 20 mg per mL Presence of Particulate Matter- Confimed customer complaint of particulates embedded in glass container and in contact with product solution. FDA Class I, its most serious class Class IFDA’s class (needs attention)May 7, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 7, 2014ClassClass IStatusTerminatedWhereNationwide
- Medicine recall Fluoxetine Capsules, USP, 20 mg, 30-count bottles Chemical Contamination: The recalling firm received notice that their supplier is recalling capsules due to complaints of capsules having an unusual odor. Class IIFDA’s classMay 7, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 7, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medicine recall Fluoxetine Capsules USP, 20 mg Chemical Contamination: Recall due to a customer complaint trend regarding capsule odor. Class IIFDA’s classMay 7, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMay 7, 2014ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medicine recall Fluoxetine Capsules USP, 10 mg, 100-count bottles Chemical Contamination: Recall due to a customer complaint trend regarding capsule odor. Class IIFDA’s classMay 7, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMay 7, 2014ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
Nothing matches all of these.
Remove a filter to see more. Each one is a fact FDA’s record publishes, so a recall can be left out because its record is silent on it.
Source:
FDA, Drug recall enforcement reports. Released Nov 3, 2026. Updated weekly.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.”
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