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 77817800 of 28,654 recalls

Medical DeviceJuly 29, 2022· Hobbs Medical, Inc.

Recalled Item: Hobbs Medical Polypectomy Snare Catalog Number: 4563 Recalled by Hobbs...

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2022· Hobbs Medical, Inc.

Recalled Item: Hobbs Posi-Stop Injection Needle Catalog Number: 4712 Recalled by Hobbs...

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2022· Hobbs Medical, Inc.

Recalled Item: Freeman Pancreatic Flexi-Stent Catalog Number: 6566 Recalled by Hobbs...

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2022· Diasol, Inc

Recalled Item: Diasol Acid Concentrate 100 Recalled by Diasol, Inc Due to Due to labeling...

The Issue: Due to labeling issue. The box label is different that the gallon label in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2022· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008T and 2008TBluestar Hemodialysis Machines with CDX-Indicated for acute...

The Issue: (1)Software version 2.74 upgrade and (2)hardware related cause that affects...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2022· BARCO NV

Recalled Item: Barco Medical Network Adapter Recalled by BARCO NV Due to installation issues

The Issue: installation issues

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2022· GELITA MEDICAL GMBH

Recalled Item: ORCA FOAM STANDARD CUBE 10x10x10 mm Recalled by GELITA MEDICAL GMBH Due to...

The Issue: In routine bioburden testing, higher than acceptable levels of Endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2022· Wright Medical Technology, Inc.

Recalled Item: Stryker SWANSON Flexspan Finger Joint Implant W/O Grommets Silicone Recalled...

The Issue: An incorrect sizing label was applied to the carton packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2022· Isopure Corp

Recalled Item: Acidified Concentrate Distribution and Storage-The Isopure ACDS (Acidified...

The Issue: Acidified Concentrate Distribution System potential electrical safety hazard...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2022· Abbott Laboratories

Recalled Item: ARCHITECT STAT Troponin-I Reagent Kit Recalled by Abbott Laboratories Due to...

The Issue: One lot of reagent was manufactured with insufficient quantities of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2022· Medtronic Neuromodulation

Recalled Item: Vanta Clinician Programmer Application Recalled by Medtronic Neuromodulation...

The Issue: Potential communication issue in which the Vanta Clinician Programmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2022· Medtronic Neuromodulation

Recalled Item: Vanta Clinician Programmer Application Recalled by Medtronic Neuromodulation...

The Issue: Potential for Vanta Clinician Programmer Application (CP App) A71200...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2022· Nobel Biocare

Recalled Item: Nobel Biocare N1 TiUltra TCC NP 3.5x13mm Recalled by Nobel Biocare Due to...

The Issue: Due to the presence of a burr which may cause an aspiration risk to patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: NARMD MEDICAL DEPOT Forceps - Kelly Straight 5.5" Recalled by Stradis...

The Issue: The sterile barrier may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: NARMD MEDICAL DEPOT Forceps - Kelly Curved 5.5" Recalled by Stradis Medical,...

The Issue: The sterile barrier may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: NARMD MEDICAL DEPOT Scissors Iris Curved 4.5" Recalled by Stradis Medical,...

The Issue: The sterile barrier may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2022· Maquet Medical Systems USA

Recalled Item: BEQ-HLS 5050 USA Recalled by Maquet Medical Systems USA Due to The firm has...

The Issue: The firm has expanded the recall for the HLS Set Advanced regarding a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2022· Maquet Medical Systems USA

Recalled Item: BEQ-HLS 7050 USA Recalled by Maquet Medical Systems USA Due to The firm has...

The Issue: The firm has expanded the recall for the HLS Set Advanced regarding a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2022· Maquet Medical Systems USA

Recalled Item: BEQ-HLS 7050 USA Recalled by Maquet Medical Systems USA Due to The firm has...

The Issue: The firm has expanded the recall for the HLS Set Advanced regarding a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2022· Maquet Medical Systems USA

Recalled Item: BEQ-HLS 5050 USA Recalled by Maquet Medical Systems USA Due to The firm has...

The Issue: The firm has expanded the recall for the HLS Set Advanced regarding a...

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

Class II — Potential Health HazardOngoing