DrugNov 12, 2025
Teva Pharmaceuticals USA Amoxicillin and Clavulanate Potassium for Oral Suspension USP, 200 recall — FDA D-0151-2026
Subpotent drug; Clavulanate Potassium component
Class IIFDA: OngoingTeva Pharmaceuticals USA, Inc
Monthly breakdown
2025 recalls by month
Select a month to review the recall records reported during that period.
December 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categoriesSeptember 2025285 records · 4 categoriesAugust 2025239 records · 4 categoriesJuly 2025370 records · 4 categoriesJune 2025342 records · 4 categoriesMay 2025258 records · 4 categoriesApril 2025302 records · 4 categoriesMarch 2025259 records · 4 categoriesFebruary 2025260 records · 4 categoriesJanuary 2025354 records · 4 categories
2025 recalls — page 26
Records are ordered by the best available source date.
VehicleNov 6, 2025
Toyota Motor Engineering & Manufacturing hard parts internal/mechanical recall — NHTSA campaign 25V767000
Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2022-2024 Toyota Tundra, Lexus LX, and 2024 Lexus GX vehicles equipped with a V35A engine. Debris from the…
hard parts internal/mechanicalToyota Motor Engineering & Manufacturing
VehicleNov 6, 2025
Chrysler frontal air bag recall — NHTSA campaign 25V765000
Chrysler (FCA US, LLC) is recalling certain 2021-2022 Ram 1500, Ram 2500, Ram 3500, Ram 4500, and Ram 5500 vehicles. The steering column control module may cause the driver's side air bag…
frontal air bagChrysler (FCA US, LLC)
Medical DeviceNov 5, 2025
CareFusion 303 Various models of BD Pyxis Medbank: Reference numbers: 1137-00 1145-00 recall — FDA Z-0367-2026
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceNov 5, 2025
CareFusion 303 All Serial Numbers/BD Pyxis CII Safe ES Tower Main, REF: 1116-00 recall — FDA Z-0371-2026
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceNov 5, 2025
Alcon Laboratories, Inc. Accessory devices for Unity and Constellation surgical consoles recall — FDA Z-0308-2026
Due to incomplete seals in the pouch which provide the sterile barrier.
Class IIFDA: OngoingAlcon Research LLC
Medical DeviceNov 5, 2025
AESCULAP SEALING UNIT FOR 10/12MM TROCARS recall — FDA Z-0311-2026
It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
Class IIFDA: OngoingAesculap Inc.
Medical DeviceNov 5, 2025
Aesculap SEALING CAP FOR 10/12MM TROCARS recall — FDA Z-0310-2026
It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
Class IIFDA: OngoingAesculap Inc.
Medical DeviceNov 5, 2025
ICU Medical ChemoLock Universal Vented Vial Spike REF: CL-70 recall — FDA Z-0343-2026
Port weld of drug transfer device may separate or break during use and potentially result in a leak.
Class IIFDA: OngoingICU Medical, Inc.
Medical DeviceNov 5, 2025
ENDOMAGNETICS Magseed Pro 7 cm soft tissue marker recall — FDA Z-0316-2026
Potential for contamination with cotton fibers.
Class IIFDA: OngoingENDOMAGNETICS LTD
Medical DeviceNov 5, 2025
ICU Medical ChemoLock Vented Vial Spike, 13mm REF: CL-72 recall — FDA Z-0345-2026
Port weld of drug transfer device may separate or break during use and potentially result in a leak.
Class IIFDA: OngoingICU Medical, Inc.
Medical DeviceNov 5, 2025
ICU Medical 60" (152 cm) Appx 1.2 ml, Ext Set, Smallbore w/ChemoLock Port, Clamp, Spiros recall — FDA Z-0339-2026
Port weld of drug transfer device may separate or break during use and potentially result in a leak.
Class IIFDA: OngoingICU Medical, Inc.
Medical DeviceNov 5, 2025
IMPRIS Imaging IMRIS Operating Suite, iMRI 3T S, containing Siemens 3 Tesla MRI Magnet recall — FDA Z-0162-2026
There is a potential safety issue associated with the magnet venting paths of the Siemens 3 Tesla MRI system within your IMRIS Operating Suite. Siemens notified IMRIS that an ice blockage…
Class IFDA: OngoingIMPRIS Imaging Inc.
Medical DeviceNov 5, 2025
Microgenics Thermo scientific MAS Omni CARDIO, Liquid Assayed Integrated Cardiac Control recall — FDA Z-0415-2026
The firm received complaints from customers reporting vial-to-vial variability when using the control with high sensitivity Troponin I assays. This defect may lead to as delay in patient…
Class IIFDA: OngoingMicrogenics Corporation
Medical DeviceNov 5, 2025
ICU Medical ChemoLock Bag Spike, 01 units REF: CL-10-10 recall — FDA Z-0328-2026
Port weld of drug transfer device may separate or break during use and potentially result in a leak.
Class IIFDA: OngoingICU Medical, Inc.
Medical DeviceNov 5, 2025
ICU Medical ChemoLock Vented Vial Spike, 20mm REF: CL-70S recall — FDA Z-0344-2026
Port weld of drug transfer device may separate or break during use and potentially result in a leak.
Class IIFDA: OngoingICU Medical, Inc.
Medical DeviceNov 5, 2025
Siemens Healthcare Diagnostics Assay: IMMULITE 2000 Intact PTH recall — FDA Z-0366-2026
The potential for falsely depressed Intact PTH patient results at the low end of the assay range, less than or equal to 50 pg/mL (less than or equal to 5.3 pmol/L), when using specific lots…
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Medical DeviceNov 5, 2025
Alcon Laboratories, Inc. Accessory devices for Unity and Constellation surgical consoles recall — FDA Z-0304-2026
Due to incomplete seals in the pouch which provide the sterile barrier.
Class IIFDA: OngoingAlcon Research LLC
Medical DeviceNov 5, 2025
ICU Medical ChemoLock Bag Spike with Clave Additive Port REF: CL3940 recall — FDA Z-0335-2026
Port weld of drug transfer device may separate or break during use and potentially result in a leak.
Class IIFDA: OngoingICU Medical, Inc.
Medical DeviceNov 5, 2025
Vantive US Healthcare Sharesource Connectivity Platform for Use with Homechoice Claria recall — FDA Z-0409-2026
Vantive has identified a software defect within the Sharesource Claria software, which may cause a patient s updated prescription program settings to not be properly saved on the actual…
Class IIFDA: OngoingVantive US Healthcare LLC
Medical DeviceNov 5, 2025
ICU Medical 7.5" (19 cm) Appx 1.5 ml, Ext Set w/ChemoLock" Port, Clamp, Graduated Adapter recall — FDA Z-0360-2026
Port weld of drug transfer device may separate or break during use and potentially result in a leak.
Class IIFDA: OngoingICU Medical, Inc.
Medical DeviceNov 5, 2025
ICU Medical Oncology Kit w/31" (79 cm) 20 Drop Admin Set w/Integrated ChemoLock" Port Drip recall — FDA Z-0334-2026
Port weld of drug transfer device may separate or break during use and potentially result in a leak.
Class IIFDA: OngoingICU Medical, Inc.
Medical DeviceNov 5, 2025
ICU Medical ChemoLock w/Mini Bag Spike ¿ REF: C-17 recall — FDA Z-0355-2026
Port weld of drug transfer device may separate or break during use and potentially result in a leak.
Class IIFDA: OngoingICU Medical, Inc.
Medical DeviceNov 5, 2025
Surgical Theater SyncAR Surgical Navigation Advanced Platform Patient Engagement recall — FDA Z-0322-2026
A software anomaly, under specific conditions when large rotational alignment values are applied in 2D Image Fusion, may lead to misalignment of any secondary image layer(s) to the primary…
Class IIFDA: TerminatedSurgical Theater Inc.
About the 2025 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.