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. 2,610 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,610 in last 12 months

Showing 1232112340 of 28,654 recalls

Medical DeviceJanuary 15, 2020· Cardinal Health 200, LLC

Recalled Item: Monoject Hypodermic Safety Needle 30G X 1/2" Item Code 1183005 Recalled by...

The Issue: Non-sterile product was shipped to customers. Product package is labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Cardinal Health 200, LLC

Recalled Item: Monoject 3mL Syringe with Hypodermic Safety Needle Recalled by Cardinal...

The Issue: Non-sterile product was shipped to customers. Product package is labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Cardinal Health 200, LLC

Recalled Item: Monoject Hypodermic Safety Needle 25G x 5/8" Item Code 1182558 Recalled by...

The Issue: Non-sterile product was shipped to customers. Product package is labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Cardinal Health 200, LLC

Recalled Item: Monoject Bluntfill with Filter Recalled by Cardinal Health 200, LLC Due to...

The Issue: Non-sterile product was shipped to customers. Product package is labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Abbott Point Of Care Inc.

Recalled Item: i-STAT CG4+ cartridge (blue) Recalled by Abbott Point Of Care Inc. Due to...

The Issue: The I-STAT BLUE CHEM8+ and CG4+ cartridges are not FDA cleared and do not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Abbott Point Of Care Inc.

Recalled Item: i-STAT CHEM8+ cartridges (blue) Recalled by Abbott Point Of Care Inc. Due to...

The Issue: The I-STAT BLUE CHEM8+ and CG4+ cartridges are not FDA cleared and do not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: Epidural Catheterization Kit with FlexTip Plus Recalled by Arrow...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: FlexTip Plus Epidural Catheterization Kit Recalled by Arrow International...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: EPIDURAL CATHETERIZATION KIT Recalled by Arrow International Inc Due to...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: EPIDURAL CATHETERIZATION KIT Recalled by Arrow International Inc Due to...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: FlexTip Plus Epidural Catheterization Set Recalled by Arrow International...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: FlexTip Plus Epidural Catheterization Set for Pediatric Lumbar Placement...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: FlexTip Plus Epidural Catheterization Set Recalled by Arrow International...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: TheraCath Epidural Catheterization Kit Recalled by Arrow International Inc...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: EPIDURAL CATHETERIZATION KIT Recalled by Arrow International Inc Due to...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: FlexTip Plus Epidural Catheterization Set Recalled by Arrow International...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: EPIDURAL CATHETERIZATION KIT Recalled by Arrow International Inc Due to...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: 10 cc Luer-Slip Loss of Resistance Syringe Recalled by Arrow International...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: EPIDURAL CATHETERIZATION KIT Recalled by Arrow International Inc Due to...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: FlexTip Plus Epidural Catheterization Kit Recalled by Arrow International...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing