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
Monthly breakdown
2026 recalls by month
Select a month to review the recall records reported during that period.
August 2026145 records · 4 categoriesJuly 2026369 records · 4 categoriesJune 2026372 records · 4 categoriesMay 2026330 records · 4 categoriesApril 2026407 records · 4 categoriesMarch 2026179 records · 4 categoriesFebruary 2026326 records · 4 categoriesJanuary 2026210 records · 4 categories
2026 recalls — page 60
Records are ordered by the best available source date.
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
Jeep Wrangler vehicle tether anchor recall — NHTSA campaign 26V224000
Chrysler (FCA US, LLC) is recalling certain 2026 Jeep Wrangler vehicles. The child seat tether welds on the second-row, right-side seat frame may be insufficient, which can reduce the…
vehicle tether anchorChrysler (FCA US, LLC)
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
Medical DeviceApr 8, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Allura Xper FD10C; System Code: 722001 recall — FDA Z-1659-2026
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
MEDLINE ANTERIOR HIP PACK DYNJ64672B recall — FDA Z-1711-2026
Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of single use biopsy valves. Potential…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceApr 8, 2026
Medtronic MiniMed MiniMed 700G Insulin Pump recall — FDA Z-1744-2026
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
Paradise Catheter recall — FDA Z-1654-2026
Due to firm distributing a nonconforming product that supposed to be scrapped and not for human use.
Class IIFDA: OngoingReCor Medical Inc.
Medical DeviceApr 8, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Vue Motion V12. Product Number: 1017979 recall — FDA Z-1692-2026
Potential that mis-ordered frames in Vue Motion during dynamic cine runs may cause images frames to display out of sequence.
Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceApr 8, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Azurion 7 M20; System Code: (1)722079, (2)722224 recall — FDA Z-1678-2026
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.
About the 2026 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.