DrugApr 15, 2026
SODIUM CHLORIDE 0.9% Sodium Chloride Injection, USP 0.9% (450 mg per 50 mL) (9 mg per mL) 50 recall — FDA D-0425-2026
Lack of Assurance of Sterility
Class IIFDA: OngoingFresenius Kabi USA, LLC
April 2026 recalls — page 9
These records include useful source details for the selected month.
DrugApr 15, 2026
SODIUM CHLORIDE 0.9% Sodium Chloride Injection, USP, 900 mg per 100 mL (9 mg per mL) 1,000 recall — FDA D-0433-2026
Lack of Assurance of Sterility
Class IIFDA: OngoingFresenius Kabi USA, LLC
DrugApr 15, 2026
DEXTROSE 5% Dextrose Injection, USP 5 g per 100 mL (50 mg per mL) 100 mL in a 100 mL recall — FDA D-0436-2026
Lack of Assurance of Sterility
Class IIFDA: OngoingFresenius Kabi USA, LLC
DrugApr 15, 2026
DEXTROSE 5% Dextrose Injection, USP 12.5 g per 250 mL (50 mg per mL) 250 mL in a 250 mL recall — FDA D-0437-2026
Lack of Assurance of Sterility
Class IIFDA: OngoingFresenius Kabi USA, LLC
DrugApr 15, 2026
Clonidine Transdermal System, USP, 0.3 mg/day, supplied in cartons of 4 Systems and 4 recall — FDA D-0474-2026
CGMP Deviations: use of an unapproved raw material
Class IIFDA: OngoingTeva Pharmaceuticals USA, Inc
DrugApr 15, 2026
DEXTROSE 5% Dextrose Injection, USP 2.5 g per 50 mL (50 mg per mL) 50 mL in a 100 mL recall — FDA D-0435-2026
Lack of Assurance of Sterility
Class IIFDA: OngoingFresenius Kabi USA, LLC
DrugApr 15, 2026
Lanreotide Injection, 120 mg/0.5 mL, Box contains 1 Pre-filled syringe, Single dose only recall — FDA D-0423-2026
Lack of Assurance of Sterility: Due to an FDA observation at the contract manufacturing site for deficiencies in their visual inspection procedure.
Class IIFDA: OngoingCipla USA, Inc.
DrugApr 15, 2026
SODIUM CHLORIDE 0.9% Sodium Chloride Injection, USP, 900 mg per 100 mL (9 mg per mL) 100 mL recall — FDA D-0430-2026
Lack of Assurance of Sterility
Class IIFDA: OngoingFresenius Kabi USA, LLC
DrugApr 15, 2026
Fagron Compounding Services Vancomycin HCI, 1.25 grams added to 250 mL, 0.9% Sodium Chloride recall — FDA D-0440-2026
Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
Class IIFDA: OngoingFagron Compounding Services
DrugApr 15, 2026
Clonidine Transdermal System, USP, 0.1 mg/day, supplied in cartons of 4 Systems and 4 recall — FDA D-0472-2026
CGMP Deviations: use of an unapproved raw material
Class IIFDA: OngoingTeva Pharmaceuticals USA, Inc
DrugApr 15, 2026
SODIUM CHLORIDE 0.9% Sodium Chloride Injection, USP, (4,500 mg per 500 mL) (9 mg per mL) 500 recall — FDA D-0428-2026
Lack of Assurance of Sterility
Class IIFDA: OngoingFresenius Kabi USA, LLC
DrugApr 15, 2026
SODIUM CHLORIDE 0.9% Sodium Chloride Injection, USP, 0.9% (900 mg per 100 mL) (9 mg per mL) recall — FDA D-0426-2026
Lack of Assurance of Sterility
Class IIFDA: OngoingFresenius Kabi USA, LLC
DrugApr 15, 2026
SODIUM CHLORIDE 0.9% Sodium Chloride Injection, USP 900 mg per 100 mL (9 mg per mL) 500 mL recall — FDA D-0432-2026
Lack of Assurance of Sterility
Class IIFDA: OngoingFresenius Kabi USA, LLC
DrugApr 15, 2026
Clonidine Transdermal System, USP, 0.2 mg/day, supplied in cartons of 4 Systems and 4 recall — FDA D-0473-2026
CGMP Deviations: use of an unapproved raw material
Class IIFDA: OngoingTeva Pharmaceuticals USA, Inc
DrugApr 15, 2026
SODIUM CHLORIDE 0.45% Sodium Chloride Injection, USP, 1.125 grams per 250 mL recall — FDA D-0424-2026
Lack of Assurance of Sterility
Class IIFDA: OngoingFresenius Kabi USA, LLC
DrugApr 15, 2026
SODIUM CHLORIDE 0.9% Sodium Chloride Injection, USP, (2,250 mg per 250 mL) (9 mg per mL) 250 recall — FDA D-0427-2026
Lack of Assurance of Sterility
Class IIFDA: OngoingFresenius Kabi USA, LLC
DrugApr 15, 2026
Fagron Compounding Services Vancomycin HCI, 1.5 grams added to 250 mL, 0.9% Sodium Chloride recall — FDA D-0441-2026
Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
Class IIFDA: OngoingFagron Compounding Services
VehicleApr 9, 2026
Chrysler instrument cluster/panel recall — NHTSA campaign 26V225000
Chrysler (FCA US, LLC) is recalling certain 2025-2026 Ram 1500 Pickup, Ram 2500 Pickup, Ram 3500 Pickup, Ram 3500 Cab Chassis, Ram 4500 Cab Chassis, and Ram 5500 Cab Chassis vehicles. A…
instrument cluster/panelChrysler (FCA US, LLC)
VehicleApr 9, 2026
Odyssey air bag control module software recall — NHTSA campaign 26V227000
Honda (American Honda Motor Co.) is recalling certain 2018-2022 Odyssey vehicles. A software programming error can cause the side and side curtain air bags to deploy unexpectedly.
air bag control module softwareHonda (American Honda Motor Co.)
Medical DeviceApr 8, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V ALLURA Xper FD10; System Code: (1) 722003, (2)722010 recall — FDA Z-1661-2026
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceApr 8, 2026
Cardinal Health Monoject Tuberculin Syringe, 1 mL Luer Lock, Catalog Number 1180100777 recall — FDA Z-1768-2026
The outer packaging and blister pack labeling identify the product as 1mL Luer Lock Tuberculin Syringe (Product Code 1180100777), however the syringes contained within the packages are…
Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceApr 8, 2026
Medtronic MiniMed MiniMed 670G Insulin Pump recall — FDA Z-1739-2026
All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when the pump is elevated…
Class IIFDA: OngoingMedtronic MiniMed, Inc.
Medical DeviceApr 8, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Azurion 7 B12; System Code: (1)722067, (2)722225 recall — FDA Z-1675-2026
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceApr 8, 2026
Synthes (USA) Products 2.4 VOLT(TM) TAP CORTEX SCREW TO 90MM recall — FDA Z-1703-2026
A full lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9 and Cortical Screw Tap 03.424.126 lot 68982P8, resulting in the bones taps having an incorrect thread.
Class IIFDA: OngoingSynthes (USA) Products LLC
How to use this monthly recall archive
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.