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Amerisource Health Services LLC

Amerisource Health Services LLC Recalls

All product recalls associated with Amerisource Health Services LLC.

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Recall Summary

Total Recalls

1000

Past Year

631

Class I (Serious)

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 61–80 of 10391 recalls

Prazosin Hydrochloride 5mg Capsules (Amerisource) – Impurity Risk (2025)

Failed Impurities/Degradation Specification: presence of N-nitroso Prazosin impurity C above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake limit

Class IIModerate

FDAOct 16, 2025Nationwide• Amerisource Health Services LLC

Prazosin Hydrochloride 1mg Capsules (Amerisource) – Impurity Risk (2025)

Failed Impurities/Degradation Specification: presence of N-nitroso Prazosin impurity C above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake limit

Class IIModerate

FDAOct 16, 2025Nationwide• Amerisource Health Services LLC

Beckman Coulter Bicarbonate Reagent (Beckman) – Result Interference (2025)

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Bicarbonate reagent may generate falsely high Bicarbonate results due to interference with Lactate Dehydrogenase (LDH) in the test sample.

Moderate

FDAOct 14, 2025Nationwide• Beckman Coulter Ireland, Inc. Lismeehan O'Callaghan'S Mills Ireland

Gabapentin Capsules (Harvard Drug) – impurity specification failure (2025)

Failed Impurities/Degradation Specifications: an out of specification result obtained during routine stability testing for Highest Unknown Impurity .

Class IIModerate

FDAOct 10, 2025Nationwide• The Harvard Drug Group LLC

Haloperidol Lactate Injection (Safecor Health) – Labeling Error (2025)

Labeling: Not Elsewhere Classified:Incorrect RFID tag labels applied to product by repackaging firm.

Class IIModerate

FDAOct 10, 2025IN, MA• Safecor Health, LLC

Gabapentin Capsules (Harvard Drug) – impurity specification failure (2025)

Failed Impurities/Degradation Specifications: an out of specification result obtained during routine stability testing for Highest Unknown Impurity .

Class IIModerate

FDAOct 10, 2025Nationwide• The Harvard Drug Group LLC

Living Glow Waist Fan (Guangzhou Jiguang) – fire hazard (2025)

Fire/Burn Risk

The recall includes the Living Glow five-in-one portable waist fan (model number CP-WFLED01). The model number is found on the label on the back of the fan. The recalled waist fan features five fan speeds, a three-mode flashlight and could be used as a power bank. The recalled fans were sold in gray, white, aqua, coral, red, and sage green. They feature a metal clip for attaching to a belt and a strap for wearing around the neck. The fans measure about 3.6 inches wide by 4 inches tall.

High

CPSCOct 9, 2025Nationwide• Guangzhou Jiguang Lighting Co. Ltd., of Guangzhou, China

Sucralfate Tablets (Amerisource) – Quality Management (2025)

CGMP Deviations: The recalling firm filed for Chapter 11 on September 30, 2024. As a result, it cannot monitor the quality program and hence cannot assure that products meet the identity, strength, quality, and purity characteristics that they are purported or represented to possess, rendering the products adulterated.

Class IIModerate

FDAOct 9, 2025Nationwide• Amerisource Health Services LLC

Roshni Cinnamon Powder (Singh Trading) – heavy metals (2025)

Product may contain elevated levels of lead and chromium.

Class IIModerate

FDAOct 9, 2025FL, MD, NC +2 more• Singh Trading Inc. DBA Roshni Foods

Quantum Intersegmental Table (Pivotal Health) – Heat Function Risk (2025)

The heat function may become damaged over time due to patients pressing on the areas with heat function components. Damage to components can lead to overheating which can lead to smoldering and melting of the vinyl cushion.

Moderate

FDAOct 9, 2025Nationwide• Pivotal Health Solutions, Inc.

TRUE METRIX Blood Glucose Meter (Trividia) – LCD display issues (2025)

Manufacturing defect causing LCD display issues with missing or partial segments (ghosting) that can result in misreading glucose values, potentially leading to inappropriate treatment decisions for diabetes management.

Moderate

FDAOct 7, 2025Nationwide• Trividia Health, Inc.

Carbidopa Levodopa Entacapone Tablets (Rising Pharma) – Product Mix-up (2025)

Product mix up: complaint received that sealed medication bottle contained Carbidopa, Levodopa, and Entacapone film-coated tablets (37.5 mg/150 mg/200 mg) instead of labelled lower strength Carbidopa, Levodopa, and Entacapone film-coated tablets (25 mg/100 mg/200 mg).

Class IIModerate

FDAOct 7, 2025Nationwide• Rising Pharma Holding, Inc.

IMMULITE 2000 Oak Mix Allergen (Siemens) – barcode scanning error (2025)

The barcode orientation on affected devices causes incorrect scanning order of tubes within the allergen holder wedge. When using an IMMULITE 2000 / IMMULITE 2000 XPi instrument in combination with a Zebra barcode scanner, the instrument will not correctly recognize the position of tubes within the allergen holder wedge.

Low

FDAOct 6, 2025Nationwide• Siemens Healthcare Diagnostics, Inc.