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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

1000

Class I (Serious)

127

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 441–460 of 25000 recalls

Chlorpromazine Tablets (Amerisource) – Foreign substance packaging (2025)

Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging at the manufacturing site, was detected with presence of a micro-organism. No micro-organism was detected on any tablets.

Class IIModerate

FDAAug 27, 2025Nationwide• Amerisource Health Services LLC

Neuroquell Supplement (Atlantic) – cGMP Violations (2025)

cGMP violations

Class IIModerate

FDAAug 27, 2025Nationwide• Atlantic Management Resources Ltd.

Cyclobenzaprine Tablets (Unichem) – Labeling Mix-Up (2025)

Labeling: Label Mix Up; Bottles of Meloxicam USP, 7.5mg, 90-count tablets (yellow in color), were labeled as Cyclobenzaprine Hydrochloride Tablets USP, 10 mg 90-count tablets (blue in color).

1...21 222324 25...1250

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Class IHigh

FDAAug 27, 2025Nationwide• Unichem Pharmaceuticals USA Inc.

Sterile Water Injection (B Braun Medical) - Sterility Concern (2025)

Lack of Assurance of Sterility- Potential for fluid leakage from the port due to port misalignment.

Class IIModerate

FDAAug 26, 2025Nationwide• B BRAUN MEDICAL INC

Sodium Chloride Irrigation (B Braun Medical) - Sterility Concern (2025)

Lack of Assurance of Sterility- Potential for fluid leakage from the port due to port misalignment.

Class IIModerate

FDAAug 26, 2025Nationwide• B BRAUN MEDICAL INC

Sonesta 6210 Fluoroscopy Table (Sonesta) – Weld Bracket Weakness (2025)

Video fluoroscopy table may contain inadequate weld on backrest bracket resulting in backrest dropping.

High

FDAAug 22, 2025NH• Sonesta Medical AB Industrivagen

MAC VU360 Cable (GE Medical) – Module Placement Risk (2025)

If a user incorrectly places the Acquisition Module into the Acquisition Module Holder, it can result in excessive bending and wear of the Acquisition Trunk Cable. This is visible as a damaged sheath or exposed wires. If a damaged Acquisition Trunk Cable is not recognized and removed from service, the cable can overheat with continued use.

High

FDAAug 22, 2025Nationwide• GE Medical Systems, LLC

Venclose digiRF Generator (Bard) – Wiring Detection Feature (2025)

Laceration Risk

Software version 3.35 of the Venclose digiRF Generator incorporates a catheter verification feature specifically designed to detect internal wiring anomalies in Venclose EVSRF Ablation Catheters prior to clinical use. This automated diagnostic check is executed immediately upon catheter connection to the generator, occurring before the procedure interface becomes accessible. When a catheter fails this verification process, the generator displays a Red X indicator on the screen without accompanying error codes, effectively disabling catheter functionality. However, BD has determined that software version 3.35 generates false positive failures due to temperature-dependent verification parameters, incorrectly flagging properly functioning Venclose EVSRF Ablation Catheters as defective when the catheter temperature is not at steady state during the check initiation.

High

FDAAug 21, 2025Nationwide• Bard Peripheral Vascular Inc 1625 W 3rd St Bldg 1 850 W. Rio Salado Prkwy. Tempe AZ 85281-2438

Chocolate Chip Cookie Dough Ice Cream (Blue Bell) – undeclared nuts (2025)

Undeclared Allergen

undeclared almond, walnut, and pecan.

Class IIModerate

FDAAug 21, 2025AL, AR, FL +14 more• Blue Bell Creameries, L.P.

Honey Balsamic Salad Kit (Taylor Farms) – undeclared allergens (2025)

Undeclared Allergen

Undeclared allergens (sesame and soy).

Class IHigh

FDAAug 21, 2025AZ, AR, CA +15 more• Taylor Farms Retail, Inc.

Aston Martin Vanquish (Aston Martin) – Vacuum Pump Failure (2025)

Aston Martin is recalling certain 2025 Vanquish vehicles. The vacuum pump may not generate vacuum, resulting in a loss of power brake assist and decreased brake function.

High

NHTSAAug 20, 2025Nationwide• ASTON MARTIN

Impella Controller (Abiomed) – Pump Driver Circuit Issue (2025)

Specific Automated Impella Controllers (AICs) that have a Pump Driver Circuit Assembly do not meet current specifications. This may lead to decreased pump performance or pump stop and trigger an Impella Failure or Impella Stopped Controller Failure alarm.

High

FDAAug 20, 2025AZ, AR, CA +14 more• Abiomed, Inc.

Sulfamethoxazole Trimethoprim Tablets (Northwind Pharmaceuticals) - Foreign Substance (2025)

Presence of a Foreign Substance: A specific lot of auxiliary polyester coil, used in product packaging by manufacturer (Amneal Pharmaceuticals LLC) was detected with presence of a micro-organism. No micro-organism was detected on any tablets.

Class IIModerate

FDAAug 20, 2025Nationwide• Northwind Pharmaceuticals LLC

Carvedilol Tablets (Harvard Drug Group) - Impurity Concern (2025)

CGMP Deviations: Results for N-Nitroso Carvedilol Impurity-1 (NNCI) impurity observed to be above the FDA-recommended limit of NMT 4.0 ppm

Class IIModerate

FDAAug 20, 2025Nationwide• The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Vacuette Serum Separator (Greiner Bio-One) – Missing Gel Separator (2025)

Some of the Vacuette CAT Serum Separator Clot Activator tubes were manufactured without gel separator, which could yield erroneous assay results and require the patient to return to the lab for recollection or repeat testing. This may result in delayed diagnosis, cause a delay in clinical decision-making or treatment and in some rare cases, yield incorrect results from less stable parameters.

Moderate

FDAAug 19, 2025AL, AR, CA +25 more• Greiner Bio-One North America, Inc.

Sand Bar Frozen Shrimp (Southwind Foods) – cesium contamination (2025)

Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137)

Class IIModerate

FDAAug 19, 2025AL, AZ, CA +6 more• Southwind Foods LLC dba Great American Seafood Imports Co.

Green Mint Chip Ice Cream (Hershey Creamery) – elevated coliform (2025)

Product tested elevated coliform counts during routine testing

Class IIModerate

FDAAug 19, 2025DE, FL, IN +4 more• HERSHEY CREAMERY CO.

Dextroamphetamine Tablets (Lannett Company) - Foreign Tablet (2025)

Presence of Foreign Tablet/Capsule: Two (2) bottles labeled as Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, 10mg, 100ct, contained one (1) tablet of Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, 5 mg.

Class IIModerate

FDAAug 19, 2025OH• Lannett Company Inc.

Frozen Cooked Shrimp (Southwind Foods) – cesium contamination (2025)

Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137)

Class IIModerate

FDAAug 19, 2025AL, AZ, CA +6 more• Southwind Foods LLC dba Great American Seafood Imports Co.

Ram 4500 (Ram) – Instrument Panel Problem (2025)

Chrysler (FCA US, LLC) is recalling certain 2026 Ram 3500, 3500 Cab Chassis, 2500, 4500 Cab Chassis, and 5500 Cab Chassis vehicles. The instrument panel may display an incorrect brake system warning light. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 101, "Control and Displays."

High

NHTSAAug 18, 2025Nationwide• RAM