DrugMay 14, 2025
BSO TESTOSTERONE PELLET 200 mg (with Cholesterol </=4%), 1 Pellet for Subcutaneous Use, This recall — FDA D-0415-2025
Presence of Particulate Matter: Glass particles were found in pellet vials.
Class IIFDA: OngoingBSO LLC
May 2025 recalls — page 8
These records include useful source details for the selected month.
DrugMay 14, 2025
Apollo Care FentaNYL 500mcg (2mcg/mL) and Ropivacaine HCl 250mg (0.1%) added to 250 mL, 0.9% recall — FDA D-0409-2025
Lack of Assurance of Sterility
Class IIFDA: OngoingApollo Care, LLC
DrugMay 14, 2025
BSO TESTOSTERONE PELLET 200 mg BLUNT, 1 Pellet for Subcutaneous Use, This is a Compounded recall — FDA D-0416-2025
Presence of Particulate Matter: Glass particles were found in pellet vials.
Class IIFDA: OngoingBSO LLC
DrugMay 14, 2025
BRS Analytical Services Carboxymethylcellulose Sodium Ophthalmic Gel 1% recall — FDA D-0405-2025
cGMP deviations and lack of assurance of sterility.
Class IIFDA: OngoingBRS Analytical Services, LLC
DrugMay 14, 2025
BSO TESTOSTERONE PELLET 100 mg (with Cholesterol </=4%), 1 Pellet for Subcutaneous Use, This recall — FDA D-0412-2025
Presence of Particulate Matter: Glass particles were found in pellet vials.
Class IIFDA: OngoingBSO LLC
DrugMay 14, 2025
Ropivacaine Hydrochloride Injection, USP, 0.5%, 500 mg per 100 mL (5mg/mL) recall — FDA D-0402-2025
Presence of Particulate Matter
Class IFDA: OngoingAmneal Pharmaceuticals, LLC
DrugMay 14, 2025
Timolol Maleate Ophthalmic Solution USP, 0.5%, Sterile, 10mL bottles recall — FDA D-0403-2025
Defective Container: Unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle.
Class IIFDA: OngoingFDC Limited
DrugMay 14, 2025
Artificial Tears Ophthalmic Solution, Dextran 70.01%/Glycerin 0.2%/Hypromellose 0.3% recall — FDA D-0404-2025
cGMP deviations and lack of assurance of sterility.
Class IIFDA: OngoingBRS Analytical Services, LLC
VehicleMay 9, 2025
Bronco camera recall — NHTSA campaign 25V312000
Ford Motor Company (Ford) is recalling certain 2021-2022 Bronco vehicles equipped with 8-inch SYNC infotainment screens that were repaired incorrectly under recall 22V-825. The rearview…
cameraFord Motor Company
VehicleMay 9, 2025
Bronco lock recall — NHTSA campaign 25V303000
Ford Motor Company (Ford) is recalling certain 2024 Bronco vehicles. The left-side rear door may be opened from the inside of the vehicle when the child safety lock is in the "ON" position.
lockFord Motor Company
VehicleMay 9, 2025
Ford upper ball joint recall — NHTSA campaign 25V310000
Ford Motor Company (Ford) is recalling certain 2024-2025 Bronco and Ranger vehicles. The front upper control arm ball joint fastener may be missing or tightened improperly, allowing the…
upper ball jointFord Motor Company
VehicleMay 9, 2025
Ford critical fasteners recall — NHTSA campaign 25V311000
Ford Motor Company (Ford) is recalling certain 2025 Ranger and Bronco vehicles. The bolts that secure the driver's seat frame to the body may be loose or missing. As such, these vehicles…
critical fastenersFord Motor Company
VehicleMay 9, 2025
Bronco lower arm recall — NHTSA campaign 25V308000
Ford Motor Company (Ford) is recalling certain 2024-2025 Bronco vehicles. The front lower control arm fasteners may not have been tightened properly, allowing the control arm to detach from…
lower armFord Motor Company
VehicleMay 9, 2025
Ford frame and members recall — NHTSA campaign 25V316000
Ford Motor Company (Ford) is recalling certain 2025 Explorer and Aviator vehicles. A mounting bolt for the front subframe may have been tightened improperly.
frame and membersFord Motor Company
VehicleMay 9, 2025
Ford back over prevention software recall — NHTSA campaign 25V315000
Ford Motor Company (Ford) is recalling certain 2021-2024 Bronco, F-150, 2021-2024 Edge, 2022-2025 Escape, F-250, F-350, F-450, F-550, F-600, 2022-2024 Expedition, 2022-2025 Transit,…
back over prevention softwareFord Motor Company
VehicleMay 9, 2025
F-150 steering recall — NHTSA campaign 25V309000
Ford Motor Company (Ford) is recalling certain 2025 F-150 vehicles. The lower intermediate shaft fasteners may be improperly attached to the steering gear, allowing the shaft to come loose…
steeringFord Motor Company
VehicleMay 8, 2025
Volvo Car USA back over prevention software recall — NHTSA campaign 25V282000
Volvo Car USA, LLC (Volvo Car) is recalling certain 2021-2025 XC40, 2022 V90, 2022-2025 S90, V90CC, C40, XC60, 2023-2025 S60, V60, V60CC, XC90, and 2025 EC40 and EX40 vehicles. The rearview…
back over prevention softwareVolvo Car USA, LLC
VehicleMay 8, 2025
Chrysler gear position indication (prndl) recall — NHTSA campaign 25V297000
Chrysler (FCA US, LLC) is recalling certain Ram 2500 and Ram 3500 vehicles equipped with a 3.5" cluster and column shifter. A software error may cause the gear selection display to be…
gear position indication (prndl)Chrysler (FCA US, LLC)
VehicleMay 8, 2025
Ram 1500 air bags recall — NHTSA campaign 25V298000
Chrysler (FCA US, LLC) is recalling certain 2019-2024 Ram 1500 vehicles. The driver's side air bag may not be connected properly, which can cause the air bag not to deploy as intended. As…
air bagsChrysler (FCA US, LLC)
Medical DeviceMay 7, 2025
Siemens Healthcare Diagnostics epoc BGEM Crea Test Card (25 pk) for the epoc Blood Analysis recall — FDA Z-1685-2025
The occurrence of discrepant high pH results in samples introduced with higher injection volumes with epoc sensor configuration 45.n.
Class IIFDA: OngoingSiemens Healthcare Diagnostics Inc.
Medical DeviceMay 7, 2025
Boston Scientific IceSeed 1.5 CX NEEDLE US, Cryoablation Needle, REF H7493967433170 recall — FDA Z-1688-2025
Boston Scientific has identified that IceSeedTM CX needles manufactured between April 2024 and February 2025 have been programmed with DEMO settings instead of Commercial settings (see…
Class IIFDA: OngoingBoston Scientific Corporation
Medical DeviceMay 7, 2025
Belmont Instrument Straight Inflow/Bifurcated Outflow Line Kit recall — FDA Z-1676-2025
Potential crack in the female connector located on the Heat Exchanger in the set, which will lead to a fluid leak through the crack during priming of the rapid infuser.
Class IIFDA: OngoingBelmont Instrument LLC
Medical DeviceMay 7, 2025
Medline procedure kits, labeled as: HAND, REF DYNJ902002J recall — FDA Z-1714-2025
It was identified that the Medline Sterile Water and Medline Sterile 0.9% Normal Saline bottles were leaking at the interface of the peel-foil and bottle opening.
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceMay 7, 2025
GE Medical Systems China Co GE Healthcare Carestation 650c A1, Model/REF Number recall — FDA Z-1634-2025
Certain Carestation 620/650/650c and 750/750c Anesthesia Delivery Systems will not provide effective ventilation in Volume Control Ventilation (VCV) mode. In these systems, effective…
Class IFDA: OngoingGE Medical Systems China Co., Ltd.
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.