Product Recalls in Oklahoma

Product recalls affecting Oklahoma — including food, drugs, consumer products, medical devices, and vehicles distributed to Oklahoma. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,642 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,642 in last 12 months

Showing 85418560 of 28,654 recalls

Medical DeviceJanuary 21, 2022· Stryker Sustainability Solutions

Recalled Item: Recalled by Stryker Sustainability Solutions Due to Mislabeling

The Issue: Mislabeling; dual-bladder tourniquet cuffs are labeled as single-bladder...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Microgenics Corporation

Recalled Item: QMS Tacrolimus Immunoassay CALIBRATOR SET QMS TACROLIMUS CAL Recalled by...

The Issue: Due to QMS Tacrolimus Calibrator recovering between 82 to 94% of their...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· SIGHT DIAGNOSTICS LTD

Recalled Item: The Sight OLO device is a computer vision based platform Recalled by SIGHT...

The Issue: In instances where custom ranges were configured on the device post...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Ventana Medical Systems Inc

Recalled Item: BenchMark ULTRA and DISCOVERY ULTRA Instruments Recalled by Ventana Medical...

The Issue: Potential for Fluid Leak inside a staining system that could cause an...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Outset Medical, Inc.

Recalled Item: Outset Tablo Console Model Number: PN-0003000 Model Number: PN-0006000...

The Issue: Due to a component in the hemodialysis console there is the possibility of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: LUMBAR PUNCTURE TRAY PEDIATRIC 21G 2.5 Recalled by Bard Peripheral Vascular...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: SAFE-T PLUS ATRAUMATIC ADULT LP TRAY Recalled by Bard Peripheral Vascular...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: SAFE-T PLUS LUMBAR PUNCTURE TRAY ADULT Recalled by Bard Peripheral Vascular...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: LUMBAR PUNCTURE DRUG FREE TRAY 22G Recalled by Bard Peripheral Vascular Inc...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: LUMBAR PUNCTURE TRAY ADULT 18G X 3.5 Recalled by Bard Peripheral Vascular...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: ADULT LUMBAR PUNCTURE DRUG FREE TRAY 20G Recalled by Bard Peripheral...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: SAFE-T PLUS LUMBARPUNCTURE TRAY ADULT Recalled by Bard Peripheral Vascular...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: ATRAUMATIC ADULT LUMBAR PUNCTURE TRAY Recalled by Bard Peripheral Vascular...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: LUMBAR PUNCTURE TRAY ADULT 20G X 3.5 DP Recalled by Bard Peripheral Vascular...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: LUMBAR PUNCTURE TRAY ADULT 22G X3.5 STRL Recalled by Bard Peripheral...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: Safe-T PLUS Pediatric/Infant Lumbar Puncture Tray Recalled by Bard...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Envisiontec US Llc

Recalled Item: PCA 4000 Curing Units Recalled by Envisiontec US Llc Due to The PCA 4000 may...

The Issue: The PCA 4000 may not fully cure EnvisionTEC dental resins to desired product...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2022· Volcano Corporation

Recalled Item: SyncVision Systems Recalled by Volcano Corporation Due to If FFR...

The Issue: If FFR measurement(s) are made prior to an iFR/FFR co-registration/pullback...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2022· Siemens Medical Solutions USA, Inc.

Recalled Item: Diagnostic Ultrasound System Recalled by Siemens Medical Solutions USA, Inc....

The Issue: The clip store function in the ultrasound imaging system does not work when...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2022· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: LINQ II Insertable Cardiac Monitor Recalled by Medtronic Inc., Cardiac...

The Issue: Devices may lose functionality due to susceptibility to moisture ingress.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing