DrugJan 22, 2025
Akron Pharma Acetaminophen Extra Strength 500 mg, 1000 Tablets per bottle, Akron Pharma recall — FDA D-0196-2025
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Class IIIFDA: OngoingAkron Pharma, Inc.
January 2025 recalls — page 9
These records include useful source details for the selected month.
DrugJan 22, 2025
Akron Pharma Diphenhydramine HCl 25 mg, 100 capsules per bottle, Akron Pharma recall — FDA D-0197-2025
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Class IIIFDA: OngoingAkron Pharma, Inc.
DrugJan 22, 2025
Akron Pharma Diphenhydramine HCl 25 mg, 1000 Capsules per bottle, Akron Pharma recall — FDA D-0198-2025
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Class IIIFDA: OngoingAkron Pharma, Inc.
VehicleJan 17, 2025
Ford 12v/24v/48v battery recall — NHTSA campaign 25V019000
Ford Motor Company (Ford) is recalling certain 2021-2023 Bronco Sport and 2022-2023 Maverick vehicles. The 12-volt battery may experience degradation and suddenly fail.
12v/24v/48v batteryFord Motor Company
VehicleJan 17, 2025
Bronco shock absorber recall — NHTSA campaign 25V025000
Ford Motor Company (Ford) is recalling certain 2021-2024 Bronco vehicles. The rear shock absorbers may corrode and fail, resulting in detachment of the external reservoir.
shock absorberFord Motor Company
VehicleJan 17, 2025
Ford automatic transmission recall — NHTSA campaign 25V020000
Ford Motor Company (Ford) is recalling certain 2025 Ford Explorer and Lincoln Aviator vehicles. The transmission may be improperly secured due to loose cross member bolts.
automatic transmissionFord Motor Company
VehicleJan 17, 2025
F-150 steering recall — NHTSA campaign 25V022000
Ford Motor Company (Ford) is recalling certain 2024 F-150 vehicles. The steering gear assembly may have been assembled with an incorrect rack, which can cause the gears to fracture.
steeringFord Motor Company
VehicleJan 16, 2025
Chrysler curtain air bag inflator recall — NHTSA campaign 25V010000
Chrysler (FCA US, LLC) is recalling certain 2016-2019 Ram 3500, Ram 1500, 2016-2020 Ram 2500, and 2016 Ram 3500 Cab Chassis vehicles. The right and left side curtain air bag inflators may…
curtain air bag inflatorChrysler (FCA US, LLC)
Medical DeviceJan 15, 2025
Applied Medical Technology AMT Mini Enteral Extension Set, 12" Right Angle Feeding Set with recall — FDA Z-0819-2025
The extension sets subject to this recall have ENFit connections, although they should have non- ENFit connections. ENFit connectors will only fit with other ENFit-compatible devices, and…
Class IIFDA: CompletedApplied Medical Technology Inc.
Medical DeviceJan 15, 2025
Maquet Cardiovascular Vasoview Hemopro 2 (w/Vasoshield) Endoscopic Vessel Harvesting System recall — FDA Z-0712-2025
Potential for two issues: 1. Bent or detached heater wire; 2. Silicone peeling or detaching from the Jaws of the Harvesting Tool
Class IFDA: OngoingMaquet Cardiovascular, LLC
Medical DeviceJan 15, 2025
Maquet Cardiovascular VasoView HemoPro 2 Endoscopic Vessel Harvesting System recall — FDA Z-0711-2025
Potential for two issues: 1. Bent or detached heater wire; 2. Silicone peeling or detaching from the Jaws of the Harvesting Tool
Class IFDA: OngoingMaquet Cardiovascular, LLC
Medical DeviceJan 15, 2025
Stryker 100V NEPTUNE 3 ROVER JAPANESE (0703-003-000) 120V NEPTUNE S ROVER (0711-001-000) recall — FDA Z-0807-2025
Bolts on the vacuum pump filter housing and the flange plate were not properly tightened, impacting the function of the Neptune rovers. Systems with loose bolts may fail to provide…
Class IIFDA: OngoingStryker Corporation
Medical DeviceJan 15, 2025
GE Medical Systems Tec 6 Plus Anesthesia Vaporizer, Reference Numbers 1107-9601-000 recall — FDA Z-0814-2025
Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series vaporizers can deliver less anesthetic agent than the vaporizer dial setting.
Class IIFDA: OngoingGE Medical Systems, LLC
Medical DeviceJan 15, 2025
Spacelabs Healthcare Xhibit Telemetry Receiver with Software, Model 96280 recall — FDA Z-0810-2025
Telemetry receivers with affected software versions may experience unsolicited system shut down and restart (Offline displayed), lasting approximately 1 to 1.5 minutes, which will cause…
Class IIFDA: OngoingSpacelabs Healthcare, Inc.
Medical DeviceJan 15, 2025
GE Medical Systems GE Healthcare Optima XR240amx, Mobile Digital Radiographic System, Model recall — FDA Z-0813-2025
GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement performed, some bolts used in the Column Safety mechanism can be missing.…
Class IIFDA: OngoingGE Medical Systems, LLC
Medical DeviceJan 15, 2025
Nipro Renal Soultions USA Citric Complete - Dry Citric Acid Concentrate recall — FDA Z-0820-2025
The outer case is mislabeled as 3.0 K, 2.0 Ca instead of 2.0 K, 3.0 Ca.
Class IIFDA: OngoingNipro Renal Soultions USA, Corporation
Medical DeviceJan 15, 2025
Elucent Medical EnVisio Patient Pad Transition Cushion recall — FDA Z-0806-2025
There is a potential safety risk caused by physical disassociation of the back section from the bed frame of Skytron model series 3600, 6500, 6600 and 6700 operating room beds when used…
Class IIFDA: OngoingElucent Medical Inc.
Medical DeviceJan 15, 2025
3B Medical, Inc. Ultrasoft Oxygen Cannula, 12 Foot Model / recall — FDA Z-0828-2025
The devices were inadvertently shipped after their expiration date.
Class IIFDA: Ongoing3B Medical, Inc.
Medical DeviceJan 15, 2025
Spacelabs Healthcare Xhibit Telemetry Receiver, Model 96280, with Service Manual recall — FDA Z-0809-2025
Telemetry receiver systems may experience a Windows proxy Issue causing the system to shut down and restart (Offline displayed), lasting approximately 1 to 1.5 minutes, which will cause…
Class IIFDA: OngoingSpacelabs Healthcare, Inc.
Medical DeviceJan 15, 2025
Qualigen The FastPack IP Sex Hormone Binding Globulin Immunoassay, Part #25000081, is for recall — FDA Z-0805-2025
Three lots of the FastPacks kitted into the FastPack SHBG Complete Kits were labeled with the incorrect expiration date. The following is a listing of affected lots: Lot Number: 2408018-1,…
Class IIIFDA: OngoingQualigen Inc.
Medical DeviceJan 15, 2025
Aerin Medical VivAer Stylus, REF CAT1785 (individual stylus), and REF CAT500 (5-pack) recall — FDA Z-0808-2025
Some units in a single production lot were programmed incorrectly which will result in the VivAer Stylus being incorrectly recognized as RhinAer Stylus when connected to the Aerin Console.
Class IIFDA: OngoingAerin Medical, Inc.
Medical DeviceJan 15, 2025
Fresenius Kabi USA Ivenix Infusion System (IIS), Large Volume Pump recall — FDA Z-0763-2025
Potential pneumatic valve failure that may cause the LVP to stop an active infusion and/or could prevent the pump from being used.
Class IFDA: OngoingFresenius Kabi USA, LLC
Medical DeviceJan 15, 2025
GE Medical Systems GE Healthcare Optima XR200amx, Mobile Digital Radiographic System, Model recall — FDA Z-0811-2025
GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement performed, some bolts used in the Column Safety mechanism can be missing.…
Class IIFDA: OngoingGE Medical Systems, LLC
Medical DeviceJan 15, 2025
GE Medical Systems GE Healthcare Optima XR220amx, Mobile Digital Radiographic System, Model recall — FDA Z-0812-2025
GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement performed, some bolts used in the Column Safety mechanism can be missing.…
Class IIFDA: OngoingGE Medical Systems, 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.