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Drug recalls

Drug recalls from FDA, newest first.
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2 recalls

Greenwich Rx Glutathione Injection

Glutathione Injection may have elevated endotoxin levels, which could cause fevers, hypotension, inflammatory reactions, anaphylactic shock and death.

FDA
Greenwich Rx Glutathione Injection

1 recall

1 recall

1 recall

2 recalls

Broadway Joe's Pain Cream

Broadway Joe's Pain Cream may be contaminated due to raw material issues.

Moderate riskFDAContamination
Broadway Joe's Pain Cream

Sage Chlorhexidine Gluconate Cloths

The 2% Chlorhexidine Gluconate Cloth, Non-sterile, 6 Disposable cloths may cause cross contamination with other products.

Moderate riskFDAContamination
Sage Chlorhexidine Gluconate Cloths

1 recall

1 recall

2 recalls

1 recall

1 recall

Adequan Canine and Equine Injections

Adequan Canine and Adequan i.m. injections contain glass fibers that may cause irritation, swelling, or infection.

Moderate riskFDAContamination
Adequan Canine and Equine Injections

1 recall

1 recall

2 recalls

2 recalls

Amneal Primidone Tablets

Primidone Tablets, USP, 50 mg may be cross-contaminated with Acemetacin API.

Low riskFDAContamination
Amneal Primidone Tablets

1 recall

1 recall

Gas-X Extra Strength Softgels

Gas-X Extra Strength Softgels may be contaminated with a diluted propylene glycol-based coolant, which could cause nausea, vomiting, abdominal pain.

High riskFDAChemical contamination
Gas-X Extra Strength Softgels

1 recall

1 recall

3 recalls

Lannett Primidone Tablets

Primidone Tablets are contaminated with trace amounts of Acemetacin.

Low riskFDAContamination
Lannett Primidone Tablets

1 recall

1 recall

1 recall

1 recall

1 recall

1 recall

1 recall

Cardinal Health Webcol Alcohol Prep Pads

Webcol Alcohol Prep pads may be non-sterile due to microbial contamination, posing an infection risk to vulnerable groups.

High riskFDASterility failure
Cardinal Health Webcol Alcohol Prep Pads

1 recall

Harbin Jixianglong Biotech Semaglutide

Reason given by FDA: CGMP Deviations This recall has been initiated due to failing to complete process validation and bacterial endotoxin method validation before distribution.

Moderate riskFDAManufacturing deviation
Drugs