Monthly recall archive

U.S. Recalls — January 2026

Complete FDA and NHTSA recall records dated in January 2026.

212recall records
4categories
Jan 7, 2026first record date
Jan 30, 2026latest record date

January 2026 recalls — page 6

These records include useful source details for the selected month.

2026 archive →
Medical DeviceJan 21, 2026

Medline Kits containing B recall — FDA Z-1051-2026

Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck…

Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJan 21, 2026

Medline Kits containing B recall — FDA Z-1057-2026

Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck…

Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJan 21, 2026

Philips Azurion Systems R3.0 recall — FDA Z-1079-2026

Nine (9) identified software issues which may result in the following: loss of X-ray after Pedal Tap, loss of X-ray after Phase Fault, missing live X-ray on the FlexVision monitor, system…

Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceJan 21, 2026

Medline Kits containing B recall — FDA Z-1055-2026

Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck…

Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJan 21, 2026

PALACOS R+G pro 40; PALACOS R+G pro 80 recall — FDA Z-1081-2026

increase of complaints regarding the breakage of the ampoules within their device systems. An extensive investigation revealed that multiple factors have an impact on the ampoule breakage.…

Class IIFDA: OngoingHeraeus Medical GmbH (Dental Division)
Medical DeviceJan 21, 2026

Medline Kits containing B recall — FDA Z-1054-2026

Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck…

Class IIFDA: OngoingMedline Industries, LP

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.