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Athenex Pharma Solutions, LLC

Athenex Pharma Solutions, LLC Recalls

All product recalls associated with Athenex Pharma Solutions, LLC.

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Recall Summary

Total Recalls

1000

Past Year

592

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 2761–2780 of 10393 recalls

Phenylephrine HCl Injection (Athenex) – Defective Container (2022)

Defective container

Class IIModerate

FDAMar 14, 2022Nationwide• Athenex Pharma Solutions, LLC

Phenylephrine HCl Injection (Athenex) – Container Defect (2022)

Defective container

Class IIModerate

FDAMar 14, 2022Nationwide• Athenex Pharma Solutions, LLC

Epinephrine Injection (Athenex) – Container Defect (2022)

Defective container

Class IIModerate

1...137 138139140 141...520

Page 139 of 520Next

FDA

Mar 14, 2022

Nationwide

• Athenex Pharma Solutions, LLC

Norepinephrine Bitartrate Injection (Athenex) – Container Defect (2022)

Defective container

Class IIModerate

FDAMar 14, 2022Nationwide• Athenex Pharma Solutions, LLC

Norepinephrine Bitartrate Injection (Athenex) – Container Defect (2022)

Defective container

Class IIModerate

FDAMar 14, 2022Nationwide• Athenex Pharma Solutions, LLC

Norepinephrine Bitartrate Injection (Athenex) – Container Defect (2022)

Defective container

Class IIModerate

FDAMar 14, 2022Nationwide• Athenex Pharma Solutions, LLC

Sucralfate Oral Suspension (DASH) – Labeling Mix-Up (2022)

Labeling: Label Mix-Up

Class IIModerate

FDAMar 11, 2022Nationwide• DASH Pharmaceuticals LLC

Gallant VR Defibrillator (St. Jude Medical) – Bluetooth Malfunction (2022)

Bluetooth malfunction impacting Gallant devices post-implant. The failure causes the device to enter an inductive-only telemetry mode with a loss of Bluetooth communication. The Bluetooth malfunction results in the inability to remotely monitor these devices and resulted in reduced battery longevity.

FDAMar 10, 2022Nationwide• St. Jude Medical, Cardiac Rhythm Management Division

Merlin PCS Programmer (St. Jude Medical) – Software Anomaly (2022)

Laceration Risk

Due to a programmer software anomaly under very specific circumstance when executing a pacing capture Decrement Test in-clinic on implantable cardioverter and cardiac resynchronization therapy defibrillator devices, the programmer may continue to execute the Decrement Test instead of terminating the test and restoring the permanent programmed pacing parameters.

FDAMar 10, 2022Nationwide• St. Jude Medical, Cardiac Rhythm Management Division

EasyFuse Dynamic Compression System (Wright Medical) – Instrument Jam Risk (2022)

The drill and adjustable drill guide can jam/bind intraoperatively resulting in the drill guide breaking.

FDAMar 10, 2022FL, NC, OH +1 more• Wright Medical Technology, Inc.

Honda Talon 1000 ROVs (American Honda) – Crash Risk (2022)

This recall involves model year 2019 - 2021 Honda Talon 1000 S2 and S4 recreational off-highway vehicles (ROVs). The vehicles were sold in various colors including red, blue, green, gray and yellow. "HONDA" is printed on the front, sides and the rear of each vehicle. "Talon" is printed on a label located on both sides of the vehicle. The Vehicle Identification Number (VIN) number is stamped on the frame on the left side under the left front fender. The VIN range for affected Talon 1000s is as shown below. MY Model VIN Start VIN End 2019 Talon 1000 S2 1HFVE05**K4000003 1HFVE05**K4003902 2020 Talon 1000 S2 1HFVE05**L4100001 1HFVE05**L4102280 2021 Talon 1000 S2 1HFVE05**M4200001 1HFVE05**M4202760 2020 Talon 1000 S4 1HFVE06**L4000002 1HFVE06**L4003420 2021 Talon 1000 S4 1HFVE06**M4100001 1HFVE06**M4102218

CPSCMar 9, 2022Nationwide• American Honda Motor Co. Inc., of Timmonsville, South Carolina