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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 661–680 of 10391 recalls

Duloxetine Capsules 30mg (Amerisource) – CGMP Impurity Limit (2024)

CGMP Deviations: Presence of N-nitroso-duloxetine impurity above the recommended interim limit.

Class IIModerate

FDADec 6, 2024Nationwide• Amerisource Health Services LLC

Duloxetine Capsules 60mg (Amerisource) – CGMP Impurity Limit (2024)

CGMP Deviations: Presence of N-nitroso-duloxetine impurity above the recommended interim limit.

Class IIModerate

FDADec 6, 2024Nationwide• Amerisource Health Services LLC

Duloxetine Capsules 30mg (Amerisource) – CGMP Impurity Limit (2024)

CGMP Deviations: Presence of N-nitroso-duloxetine impurity above the recommended interim limit.

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Class II

Moderate

FDADec 6, 2024Nationwide• Amerisource Health Services LLC

Cascade Raw Cheddar (Heber Valley) – E. coli risk (2024)

E. coli

The Cascade Raw Cheddar Cheese was recalled due to Shiga toxin-producing E. coli (STEC) and elevated generic E.coli in finished product testing results.

Class IHigh

FDADec 6, 2024MT, NV, UT +1 more• Heber Valley Artisan Cheese, LLC.

Cucumber Select (Hardies Fresh Foods) – Salmonella Risk (2024)

Salmonella

Cucumbers have the potential to be contaminated with Salmonella

Class IHigh

FDANov 27, 2024TX• HARDIES FRESH FOODS

Xhibit Telemetry Receiver (Spacelabs) – Windows Proxy Issue (2024)

Telemetry receiver systems may experience a Windows proxy Issue causing the system to shut down and restart (Offline displayed), lasting approximately 1 to 1.5 minutes, which will cause temporary loss of monitoring. If a clinical event occurred during this period, staff may not detect until the system restarts; necessary clinical intervention could be delayed.

High

FDANov 25, 2024AL, AK, AZ +41 more• Spacelabs Healthcare, Inc.

Eclipse PRO Holter Recorder (Spacelabs) – Serial Number Error (2024)

Due to a manufacturing error the incorrect device serial number was potentially programmed into the holter recorder. The physical serial number label on the device might not match the serial number programmed into the device.

Low

FDANov 25, 2024AR, CA, CO +19 more• Spacelabs Healthcare, Ltd. Unit B Foxholes Centre; John Tate Road Hertford United Kingdom

Eclipse Mini Holter Recorder (Spacelabs) – Serial Number Error (2024)

Low

FDANov 25, 2024AR, CA, CO +19 more• Spacelabs Healthcare, Ltd. Unit B Foxholes Centre; John Tate Road Hertford United Kingdom

Xhibit Telemetry Receiver (Spacelabs) – System Shutdown Risk (2024)

Telemetry receivers with affected software versions may experience unsolicited system shut down and restart (Offline displayed), lasting approximately 1 to 1.5 minutes, which will cause temporary loss of monitoring. If a clinical event occurred during this period, staff may not detect until the system restarts and necessary clinical intervention could be delayed.

High

FDANov 25, 2024AL, AR, CO +24 more• Spacelabs Healthcare, Inc.

Clarity Precision Grip Attachments (3M) – Tooth Mating Issue (2024)

Attachments may not mate with the tooth as intended in the digital treatment design.

Moderate

FDANov 22, 2024Nationwide• 3M Company Health Care Business 3m Center

VCF Contraceptive Gel (Apothecus) – Assay Deviation (2024)

CGMP deviations: out of specifications for assay

Class IIModerate

FDANov 22, 2024Nationwide• Apothecus Pharmaceutical Corp.

Epoc NXS Host (Siemens) – Software Malfunction (2024)

Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System because of a software malfunction that occurs when specific criteria are met that can result in the incorrect patient name being assigned to a blood measurement by the device if the user of the device does not ensure verification of the correct patient name. The software malfunction has the potential to impact patient safety via misdiagnosis and/or mistreatment by a clinician if the wrong patient information is saved with the test result from the subject device.

High

FDANov 22, 2024Nationwide• Siemens Healthcare Diagnostics, Inc.

Nerf Barrage Bike Helmets – Head Injury Risk (2024)

This recall involves Nerf Barrage Youth bike helmets. The helmets have a blue/orange exterior, black straps, an orange buckle, and are size medium (M). NERF is printed in white lettering on the sides of the helmet. Model 6011 is printed on a label on the inside of the helmet. The lot number (LOT#) and reference number (REF#) can be found on the same label on the inside of the helmet. Only helmets with LOT# BC01BJ01-200623 and REF# 5382-BL and LOT# BC01BJ01-111521 and REF# 4970-BL are included in this recall.

High

CPSCNov 21, 2024Nationwide• Jingzhou Taike Sport Equipment Co. Ltd, of China

Philips Smart-Hopping AP (Philips) – Channel Setting Problem (2024)

The following four issues are included: 1. Certain Channel Settings may result in an Access Point preventing a connected client device from roaming to another Access Point potentially causing the client device to appear to drop out from the network. 2. if the Access Point experiences a disconnection from the Access Point Controller exceeding 4 minutes, the Access Point may not transition through the desired state to all for clean reconnection of the client radio link. 3. Potential to experience higher than expected data dropouts, device disassociations/reassociations for their wireless clients, and frequent "Loss of AP" alerts. 4. Potential for the Smart-hopping Access Point is affected by a software issue where the Access Point will resent after 82.85 days when the frame counter reaches its limit. This causes the latest synchronization check to fail and potential for loss of patient data.

Moderate

FDANov 20, 2024Nationwide• Philips North America Llc

VACUETTE SAFELINK (Greiner Bio-One) – Blood Leakage Risk (2024)

The VACUETTE SAFELINK Holder with male luer lock may leak blood due to the protective rubber sleeve bunching up and not retracting when using the device.

Moderate

FDANov 19, 2024Nationwide• Greiner Bio-One GmbH Bad Haller Strase

Intracardiac Sucker (Med Michigan) – Pouch Seal Defect (2024)

Incomplete or partial pouch seals, which may result in a breach in the sterility.

Moderate

FDANov 19, 2024IL, IN• Med Michigan Holding Llc

Baxter SIGMA Spectrum Pump (Baxter) – Incomplete Testing (2024)

Devices were identified as released after repair without full testing being performed, which includes flow testing.

High

FDANov 19, 2024Nationwide• Baxter Healthcare Corporation

Duloxetine DR Capsules 60mg (Rising Pharma) – N-nitroso Impurity (2024)

CGMP Deviations: Presence of N-nitroso-duloxetine impurity above recommended interim limit

Class IIModerate

FDANov 19, 2024Nationwide• Rising Pharma Holding, Inc.

Duloxetine DR Capsules 20mg (Rising Pharma) – N-nitroso Impurity (2024)

CGMP Deviations: Presence of N-nitroso-duloxetine impurity above recommended interim limit

Class IIModerate

FDANov 19, 2024Nationwide• Rising Pharma Holding, Inc.

Duloxetine DR Capsules 30mg (Rising Pharma) – N-nitroso Impurity (2024)

CGMP Deviations: Presence of N-nitroso-duloxetine impurity above recommended interim limit

Class IIModerate

FDANov 19, 2024Nationwide• Rising Pharma Holding, Inc.