DrugDec 21, 2022
Lacosamide Oral Solution, USP, CV, 10mg/mL recall — FDA D-0094-2023
Failed Excipient Specifications: out of specification result observed for p-Hydroxybenzoic Acid content
Class IIIFDA: TerminatedCamber Pharmaceuticals, Inc.
Latest records
Latest recalls — page 646
The newest recall records with useful source details are listed here.
VehicleDec 19, 2022
BMW critical fasteners recall — NHTSA campaign 22V942000
BMW of North America, LLC (BMW) is recalling certain 2023 X5 sDrive40i, X5 M50i and X5 xDrive 45e vehicles. One of the four bolts that connects the backrest to the driver's seat frame may…
critical fastenersBMW of North America, LLC
VehicleDec 15, 2022
General Motors front passenger recall — NHTSA campaign 22V929000
General Motors, LLC (GM) is recalling certain 2023 Chevrolet Equinox and GMC Terrain vehicles equipped with ventilated front passenger seats. The Occupant Classification System may not…
front passengerGeneral Motors, LLC
Medical DeviceDec 14, 2022
Remel Thermo SCIENTIFIC Sensititre Plate, GN4F, Gram Negative IVD AST recall — FDA Z-0327-2023
An internal technical investigation has confirmed that Thermo Scientific" Gram Negative IVD AST Sensititre Plate may lead to false susceptible results for Proteae Tribe (including Proteus…
Class IFDA: TerminatedRemel Inc.
Medical DeviceDec 14, 2022
Integrity Implants LineSider Spinal System 5.5/6.0mm, Non-mod Standard 7.1mm - Dual Lead recall — FDA Z-0418-2023
Potential for weld separation of the Upper Tulip Head component from the Lower Tulip Head component, which would result in the separation of the Tulip Head from the Screw Shank.
Class IIFDA: TerminatedIntegrity Implants Inc.
Medical DeviceDec 14, 2022
Qvella The FAST System and the FAST PBC Prep Cartridge together are a closed, rapid and recall — FDA Z-0425-2023
Device exceeds the limitations of a Class I 510(k)-exempt device so the user manual, instructions for use, and promotional materials are being corrected to remove all references to…
Class IIFDA: OngoingQvella Corporation
Medical DeviceDec 14, 2022
Cardinal Health Dover Closed Urethral Tray with Hydrogel Coated Red Rubber Catheter 16 Fr/Ch recall — FDA Z-0357-2023
Occlusion (blockage) of the bubble inlet port of the urinary drainage bag which may prevent urine draining into the bag. If the bladder is not emptied within a clinically appropriate time,…
Class IIFDA: OngoingCardinal Health
Medical DeviceDec 14, 2022
Olympus Corporation of the Americas HF Resection Electrodes, Model Numbers WA22602S recall — FDA Z-0424-2023
An incompatible HF cable may be packaged with the HF Resection Electrodes. This cable cannot be connected to the electrosurgical generator and may lead to delay or cancellation of the…
Class IIFDA: OngoingOlympus Corporation of the Americas
Medical DeviceDec 14, 2022
Insulet Omnipod 5 Automated Insulin Delivery System Product catalog numbers: PT-000409: ASM recall — FDA Z-0423-2023
The firm has become aware of an issue with the Omnipod 5 Controller where the Controller charging port and charging cable are melting, deforming, or discoloring due to heat generated by…
Class IIFDA: OngoingInsulet Corporation
Medical DeviceDec 14, 2022
CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS, 1.0MM TIP OVERALL recall — FDA Z-0396-2023
BD has determined that the Instructions For Use (IFU) provided by BD is missing certain content that is contained in the manufacturer's IFU. This missing content is related to the interface…
Class IIFDA: OngoingCarefusion 2200 Inc.
Medical DeviceDec 14, 2022
CareFusion V. Mueller ROUND HANDLE BAYONET BIPOLAR FORCEPS, 1.0MM TIP OVERALL LENGTH 10-1/2" recall — FDA Z-0406-2023
BD has determined that the Instructions For Use (IFU) provided by BD is missing certain content that is contained in the manufacturer's IFU. This missing content is related to the interface…
Class IIFDA: OngoingCarefusion 2200 Inc.
Medical DeviceDec 14, 2022
Bunnell 2.5 mm LifePort Endotracheal Tube Adapters 10-pack, Catalog: 9025 recall — FDA Z-0371-2023
Some adaptors, for use with high frequency ventilators, were packaged improperly, and may deform at the tip, which may impair the ability to pass a suction catheter or may affect normal…
Class IIFDA: OngoingBunnell, Inc.
Medical DeviceDec 14, 2022
CareFusion V. Mueller Neuro/Spine TITANUIM BIPOLAR FORCEPS STRAIGHT, 0.25MM TIP OVERALL recall — FDA Z-0412-2023
BD has determined that the Instructions For Use (IFU) provided by BD is missing certain content that is contained in the manufacturer's IFU. This missing content is related to the interface…
Class IIFDA: OngoingCarefusion 2200 Inc.
Medical DeviceDec 14, 2022
CareFusion V. Mueller TITANIUM BAYONET IRRIGATING BIPOLAR FORCEPS INSULATED STRAIGHT FINE recall — FDA Z-0414-2023
BD has determined that the Instructions For Use (IFU) provided by BD is missing certain content that is contained in the manufacturer's IFU. This missing content is related to the interface…
Class IIFDA: OngoingCarefusion 2200 Inc.
Medical DeviceDec 14, 2022
FULL VISION INC. TRACKMASTER, TREADMILL TMX428 110V, Model #317-07926 recall — FDA Z-0364-2023
This has been identified a rare occurrence, under a specific scenario, where the circuit is found in a latch-up condition on the PCB that controls the safety function of the Magnetic Safety…
Class IIFDA: OngoingFull Vision Inc.
Medical DeviceDec 14, 2022
CareFusion V. Mueller Neuro/Spine TITANIUM BAYONET INSULATED IRRIGATING BIPOLAR FORCEPS recall — FDA Z-0416-2023
BD has determined that the Instructions For Use (IFU) provided by BD is missing certain content that is contained in the manufacturer's IFU. This missing content is related to the interface…
Class IIFDA: OngoingCarefusion 2200 Inc.
Medical DeviceDec 14, 2022
FULL VISION INC. TRACKMASTER, TREADMILL TMX428CP 110V, Model #317-07928 recall — FDA Z-0366-2023
This has been identified a rare occurrence, under a specific scenario, where the circuit is found in a latch-up condition on the PCB that controls the safety function of the Magnetic Safety…
Class IIFDA: OngoingFull Vision Inc.
Medical DeviceDec 14, 2022
CareFusion V. Mueller TITANIUM BAYONET BIPOLAR FORCEPS, 1.5MM TIP, STRAIGHT STANDARD, 8-3/4" recall — FDA Z-0408-2023
BD has determined that the Instructions For Use (IFU) provided by BD is missing certain content that is contained in the manufacturer's IFU. This missing content is related to the interface…
Class IIFDA: OngoingCarefusion 2200 Inc.
Medical DeviceDec 14, 2022
CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS 0.7MM TIP OVERALL LENGTH recall — FDA Z-0401-2023
BD has determined that the Instructions For Use (IFU) provided by BD is missing certain content that is contained in the manufacturer's IFU. This missing content is related to the interface…
Class IIFDA: OngoingCarefusion 2200 Inc.
Medical DeviceDec 14, 2022
Carefusion V. Mueller GERALD BAYONET IRRIGATING BIPOLAR FORCEPS 1.0MM TIP OVERALL LENGTH recall — FDA Z-0385-2023
BD has determined that the Instructions For Use (IFU) provided by BD is missing certain content that is contained in the manufacturer's IFU. This missing content is related to the interface…
Class IIFDA: OngoingCarefusion 2200 Inc.
Medical DeviceDec 14, 2022
CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS 1.5MM TIP OVERALL LENGTH recall — FDA Z-0403-2023
BD has determined that the Instructions For Use (IFU) provided by BD is missing certain content that is contained in the manufacturer's IFU. This missing content is related to the interface…
Class IIFDA: OngoingCarefusion 2200 Inc.
Medical DeviceDec 14, 2022
Integrity Implants LineSider Spinal System pedicle screws, 5.5/6.0mm, Non-mod Standard 7.1mm recall — FDA Z-0421-2023
Potential for intraoperative screw head separation at weld location.
Class IIFDA: TerminatedIntegrity Implants Inc.
Medical DeviceDec 14, 2022
Carefusion V. Mueller HARDY BAYONET BIPOLAR FORCEPS WITH STOP, 0.5MM TIP OVERALL LENGTH recall — FDA Z-0376-2023
BD has determined that the Instructions For Use (IFU) provided by BD is missing certain content that is contained in the manufacturer's IFU. This missing content is related to the interface…
Class IIFDA: OngoingCarefusion 2200 Inc.
Medical DeviceDec 14, 2022
Carefusion V. Mueller JEWELERS BIPOLAR FORCEPS 0.4MM TIP, STRAIGHT OVERALL LENGTH 4" recall — FDA Z-0392-2023
BD has determined that the Instructions For Use (IFU) provided by BD is missing certain content that is contained in the manufacturer's IFU. This missing content is related to the interface…
Class IIFDA: OngoingCarefusion 2200 Inc.
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
October 2026110 records · 3 categoriesSeptember 2026364 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 categories