American Regent recalls
23 federal recalls on file, showing the 16 from the last 12 months. We monitor every CPSC, FDA, USDA, and NHTSA notice for American Regent and translate it into plain English — free weekly digest, optional same-day alerts.
- 2026-09-16FDA-DrugClass IAmerican Regent epinephrine injection recalled for contamination
American Regent's epinephrine injection (1 mg/mL, 30 mL vials) may contain particulate matter—including nylon, glass, and other materials—and some vials are broken or leaking. This affects the sterility and safety of the medication. Three specific lot numbers distributed nationwide are involved.
- 2026-09-03FDA-PRAmerican Regent epinephrine injection recalled for particulate contamination
American Regent is recalling three lots of epinephrine injection (1 mg/mL multi-dose vials) due to leaking and cracked vials, plus contamination with particles including nylon, cellulosic, acrylic, polyethylene, and glass. These particles can block blood vessels, cause blood clots, and damage organs; cracked vials also risk loss of sterility and bacterial contamination. No adverse events have been reported so far.
- 2026-08-26FDA-DrugClass IIAmerican Regent niCARdipine injection recalled for particulate matter
American Regent's niCARdipine Hydrochloride Injection (25 mg/10mL) has been recalled due to contamination with particulate matter, including hair, glass, and/or paraformaldehyde. The affected lot (25295N0C0, expiring 04/30/2027) was distributed nationwide and affects approximately 43,460 vials.
- 2026-08-26FDA-DrugClass IIAmerican Regent Tralement injection recalled for particulate matter
American Regent's Tralement (trace elements injection) contains particulate matter including hair, glass, and/or paraformaldehyde. The contamination affects specific lots with expiration dates in April and September 2027. This is a prescription medication used in clinical settings.
- 2026-08-26FDA-DrugClass IAmerican Regent Papaverine HCl Injection recalled for particulate contamination
American Regent's Papaverine HCl Injection (60 mg/2 mL) has been found to contain particulate matter identified as glass and/or paraformaldehyde. The contamination affects one lot (25202, expiring 11/30/2026) distributed nationwide. This is a prescription injectable medication used to treat certain circulatory conditions.
- 2026-08-26FDA-DrugClass IIAmerican Regent Multrys injection recalled for particulate contamination
American Regent is recalling Multrys (Trace Elements Injection 4, USP) due to contamination with particulate matter, including hair, glass, and/or paraformaldehyde. The contamination was identified in specific lot 25163 (expiration 4/30/2027). This is a prescription intravenous medication used in hospitals and clinical settings.
- 2026-08-26FDA-DrugClass IIAmerican Regent Selenious Acid Injection recalled for contamination
American Regent's Selenious Acid Injection (a trace mineral used in intravenous nutrition) has been recalled because some vials contain particulate matter, including hair, glass, and/or paraformaldehyde. The contamination affects specific lot numbers distributed nationwide.
- 2026-08-26FDA-DrugClass IIAmerican Regent acetylcysteine solution recalled for particulate contamination
American Regent's acetylcysteine solution (20%, 200 mg/mL) in 4 mL vials has been found to contain particulate matter including hair, glass, and/or paraformaldehyde. The contamination affects two lots distributed nationwide. This is a prescription-only inhalation medication.
- 2026-08-26FDA-DrugClass IIAmerican Regent acetylcysteine solution recalled for particulate contamination
American Regent's acetylcysteine solution (10%, 100 mg/mL) in 4 mL vials has been found to contain particulate matter, including hair, glass, and/or paraformaldehyde. The contamination affects three specific lots distributed nationwide. This is a prescription medication for inhalation use only.
- 2026-08-26FDA-DrugClass IIAmerican Regent Atropine Sulfate injection recalled for contamination
American Regent's Atropine Sulfate injection (1 mg/mL) has been found to contain particulate matter, including hair, glass, and/or paraformaldehyde. The contamination affects specific lot 24353 (expiration 9/30/2026). This is a prescription injectable medication used in hospitals and clinical settings.
- 2026-08-26FDA-DrugClass IIAmerican Regent aminocaproic acid injection recalled for contamination
American Regent's aminocaproic acid injection (250 mg/mL) has been recalled because batches contain particulate matter including hair, glass, and/or paraformaldehyde. The contamination affects 20 mL vials distributed nationwide. This is a prescription medication used to control bleeding.
- 2026-08-26FDA-DrugClass IIAmerican Regent cyanocobalamin injection recalled for particulate contamination
American Regent's cyanocobalamin (vitamin B12) injection has been recalled due to contamination with particulate matter, including hair, glass, and/or paraformaldehyde. The affected product is a 10,000 mcg/10 mL multi-dose vial (Lot #25082, expiring 3/31/2027). This is a prescription medication administered by injection.
- 2026-08-26FDA-DrugClass IIAmerican Regent Cyanocobalamin injection recalled for contamination
American Regent's Cyanocobalamin injection (vitamin B12) has been found to contain particulate matter, including hair, glass, and paraformaldehyde. The contamination affects specific lot numbers distributed nationwide. This is a prescription medication given by injection.
- 2026-08-26FDA-DrugClass IIAmerican Regent nitroglycerin injection recalled for particulate contamination
American Regent's nitroglycerin injection (50 mg/10 mL vials) has been found to contain particulate matter, including hair, glass, and/or paraformaldehyde. This affects lot #24291 with an expiration date of 8/31/2026, distributed nationwide. The contamination was discovered during quality testing.
- 2026-07-31FDA-PRAdequan Canine and i.m. injections recalled for glass fiber contamination
American Regent, Inc. Animal Health recalled four specific lots of Adequan Canine Injection (for dogs) and Adequan i.m. Injection (for horses) after discovering glass fibers in the products during internal testing. No adverse events have been reported to date.
- 2026-07-24FDA-PRAmerican Regent Papaverine Injection recalled for glass particles
American Regent identified glass and paraformaldehyde particles in one lot of Papaverine Hydrochloride Injection (Lot #25202), a prescription medication used to improve blood circulation and treat muscle spasms. The particles could cause local irritation, blood vessel blockage, and serious complications including stroke.
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