DrugMar 19, 2025
Johnson, S C and Son Kids by babyganics SPF 50 mineral sunscreen totally tropical recall — FDA D-0276-2025
Chemical Contamination
Class IIFDA: OngoingJohnson, S C and Son, Inc
Latest records
Latest recalls — page 251
The newest recall records with useful source details are listed here.
DrugMar 19, 2025
Livalo (pitavatstatin) tablets, 4 mg, 90-count bottles recall — FDA D-0258-2025
Presence of foreign tablets/capsules
Class IIIFDA: CompletedKowa Pharmaceuticals America
DrugMar 19, 2025
Aspen Biopharma Labs Pvt Finasteride NDC# 82187-1003-1 Container Description: The product recall — FDA D-0262-2025
CGMP Deviations
Class IIFDA: OngoingAspen Biopharma Labs Pvt., Ltd.
DrugMar 19, 2025
Chattem Unisom, SleepMelts, Diphenhydramine HCl tablets, 25 mg, Nighttime Sleep-Aid, 4 x 8 recall — FDA D-0266-2025
CGMP Deviations: Nitrosamine Drug Substance Related Issue impurity above the daily acceptable intake limit defined by the Food and Drug Administration.
Class IIFDA: OngoingChattem Inc
VehicleMar 14, 2025
CX-50 trailer hitch recall — NHTSA campaign 25V167000
Mazda North American Operations (Mazda) is recalling certain 2024-2025 CX-50 vehicles equipped with Mazda Genuine Accessory trailer hitches. The trailer hitch assembly bolts may loosen and…
trailer hitchMazda North American Operations
VehicleMar 14, 2025
Ford control module (tcm/pcm/tecm) recall — NHTSA campaign 25V158000
Ford Motor Company (Ford) is recalling certain 2021-2024 Bronco Sport and 2022-2023 Maverick vehicles previously repaired incorrectly under recall number 24V-267. The body and power train…
control module (tcm/pcm/tecm)Ford Motor Company
VehicleMar 14, 2025
Ford fuel injection system recall — NHTSA campaign 25V165000
Ford Motor Company (Ford) is recalling certain 2020-2022 Escape and 2021-2023 Bronco Sport vehicles previously repaired incorrectly under recall numbers 22V-859 or 24V-187. A fuel injector…
fuel injection systemFord Motor Company
VehicleMar 14, 2025
Escape camera recall — NHTSA campaign 25V161000
Ford Motor Company (Ford) is recalling certain 2025 Escape vehicles. The rearview camera may incorrectly display an inverted image when the vehicle is in reverse. As such, these vehicles…
cameraFord Motor Company
VehicleMar 14, 2025
Explorer driveshaft recall — NHTSA campaign 25V166000
Ford Motor Company (Ford) is recalling certain 2020-2022 Explorer vehicles previously repaired incorrectly under recall numbers 23V-199 or 22V-255. The rear axle horizontal mounting bolt…
driveshaftFord Motor Company
VehicleMar 14, 2025
Ford back over prevention software recall — NHTSA campaign 25V159000
Ford Motor Company (Ford) is recalling certain 2020-2023 Explorer, Lincoln Aviator, and 2020-2022 Lincoln Corsair vehicles previously repaired incorrectly under recall number 23V-342. The…
back over prevention softwareFord Motor Company
VehicleMar 14, 2025
F-150 control module (tcm/pcm/tecm) recall — NHTSA campaign 25V169000
Ford Motor Company (Ford) is recalling certain 2021 F-150 vehicles previously repaired incorrectly under recall number 22V-188. The Diagnostic Trouble Code (DTC) for low transmission fluid…
control module (tcm/pcm/tecm)Ford Motor Company
VehicleMar 14, 2025
Ford valves/valve body recall — NHTSA campaign 25V164000
Ford Motor Company (Ford) is recalling certain 2024-2025 F-150, Bronco, 2024 Ranger, 2025 Mustang, Explorer, and Aviator vehicles. The transmission valve body may have been machined…
valves/valve bodyFord Motor Company
Medical DeviceMar 12, 2025
Hiossen Osstem Implant System - Abutment: ET Multi AbutmentSize: 4.8D 5.0GH - Abutment is recall — FDA Z-1276-2025
Patient chart stickers provided inside the packaging may incorrectly identify ET Rigid Abutments as Regular version whereas the actual product is a Mini version; and identify the ET Multi…
Class IIFDA: OngoingHiossen Inc.
Medical DeviceMar 12, 2025
Philips IntelliSpace Cardiovascular software, Model 830089 recall — FDA Z-1252-2025
Study data is not able to be archived, copied, or exported with the cardiovascular software version.
Class IIFDA: OngoingPhilips Medical Systems Nederland B.V.
Medical DeviceMar 12, 2025
TAS Medical TISSUE APPROXIMATION SYSTEM (TAS), Models T-4000, T-5000, T-LAP recall — FDA Z-1294-2025
Tissue approximation straps (zip-ties) have broken before or during implantation so firm developed an interim zip-tie conditioning method submerging zip-ties in 104-degrees F sterile saline…
Class IIFDA: OngoingTAS Medical Inc.
Medical DeviceMar 12, 2025
Medtronic MiniMed MiniMed insulin pump, REF: 780G recall — FDA Z-1266-2025
All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and 7XX series) were found to have the potential for abnormal insulin delivery due to changes in air pressure, which…
Class IIFDA: OngoingMedtronic MiniMed, Inc.
Medical DeviceMar 12, 2025
Alcon Custom Pak with Non-Latex Symbol, Pak: 12771-18, 18050-10, 18252-17, 12698-09 recall — FDA Z-1293-2025
Customer-designed sterile surgical procedure packs contain latex components as specified; but, the content label sealed within the transparent sterile pouch contains the symbol for a…
Class IIFDA: OngoingAlcon Research LLC
Medical DeviceMar 12, 2025
DeRoyal REF 71-C5100NS Tubing, Suction, Connector recall — FDA Z-1291-2025
Due to the inner diameter of the suction tubing connector being smaller than the suction canister lid port connection. This size difference, combined with the durometer of the plastic…
Class IIFDA: OngoingDeRoyal Industries Inc.
Medical DeviceMar 12, 2025
Biosense Webster VARIPULSE Bi-Directional Ablation Catheter REF D141201 recall — FDA Z-1205-2025
Due to an observed trend of neurovascular events
Class IFDA: OngoingBiosense Webster, Inc.
Medical DeviceMar 12, 2025
LUMENIS (1) Lumenis Pulse 120H 30 amp, REF GA 2009996, Laser System recall — FDA Z-1290-2025
The initial current in certain chargers may lead to overheating and damage to the power resistors on the Alternating Current (AC) controller during the power-on sequence of the laser…
Class IIFDA: OngoingLUMENIS, LTD.
Medical DeviceMar 12, 2025
Medtronic MiniMed MiniMed insulin pump, REF: 700G recall — FDA Z-1262-2025
All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and 7XX series) were found to have the potential for abnormal insulin delivery due to changes in air pressure, which…
Class IIFDA: OngoingMedtronic MiniMed, Inc.
Medical DeviceMar 12, 2025
Medtronic MiniMed MiniMed insulin pump, REF: 740G recall — FDA Z-1264-2025
All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and 7XX series) were found to have the potential for abnormal insulin delivery due to changes in air pressure, which…
Class IIFDA: OngoingMedtronic MiniMed, Inc.
Medical DeviceMar 12, 2025
Medtronic MiniMed MiniMed insulin pump, REF: 670G recall — FDA Z-1261-2025
All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and 7XX series) were found to have the potential for abnormal insulin delivery due to changes in air pressure, which…
Class IIFDA: OngoingMedtronic MiniMed, Inc.
Medical DeviceMar 12, 2025
Telcare Philips Connected Blood Glucose Meter, BGM 4 recall — FDA Z-1270-2025
Telcare, LLC has received customer complaints related to battery expansion/swelling for its Philips Connected Blood Glucose Meter (i.e., BGM 4 brand name) Monitoring System.. The issue was…
Class IIFDA: OngoingTelcare, LLC
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Recent recall archives
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September 2026363 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categories