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. 2,120 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,120 in last 12 months

Showing 32813300 of 28,654 recalls

Medical DeviceJuly 31, 2024· Medtronic MiniMed, Inc.

Recalled Item: MiniMed Insulin Pump Device. MiniMed 670G Recalled by Medtronic MiniMed,...

The Issue: Insulin pumps that have been dropped, bumped, or experienced physical impact...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 30, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista¿ Total Bilirubin (TBIL) Flex Reagent Cartridge Recalled by...

The Issue: During manufacturing, the last three tests from the 160 test flex of lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2024· Agfa N.V.

Recalled Item: DR 800. Digital Radiography X-ray System. Recalled by Agfa N.V. Due to...

The Issue: Potential for the front lever chain of the DR 800 table to fail.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Urinary/Cerebrospinal Fluid Protein (UCFP) Recalled by Siemens...

The Issue: The potential for biased quality control (QC) and patient results when using...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Urinary/Cerebrospinal Fluid Protein (UCFP) Recalled by...

The Issue: The potential for biased quality control (QC) and patient results when using...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...

The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...

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

Class II — Potential Health HazardOngoing