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. 2,590 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,590 in last 12 months

Showing 1558115600 of 49,976 recalls

Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic HY10J00R12 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic HY11B40R1 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic HY10Y54R4 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Covidien, LP

Recalled Item: HME for Tracheostomized Patients Recalled by Covidien, LP Due to The company...

The Issue: The company was notified by their supplier of sterilization services for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic CB10R55R5 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic 1A46R11 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic HY7M07R6 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic CB1H18R20 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic HY8M63R4 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic HY8R62R13 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
DrugApril 28, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: Sodium Chloride 0.9% Recalled by Fresenius Medical Care Holdings, Inc. Due...

The Issue: Temperature Abuse: Product exposed to temperature outside specified limits.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 28, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: DELFELX Peritoneal Dialysis Solution with 4.25% Dextrose Recalled by...

The Issue: Temperature Abuse: Product exposed to temperature outside specified limits.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugApril 28, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: DELFLEX Peritoneal Dialysis Solution with 4.25% Dextrose Recalled by...

The Issue: Temperature Abuse: Product exposed to temperature outside specified limits.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugApril 28, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: DELFLEX Peritoneal Dialysis Solution with 2.5 % Dextrose Recalled by...

The Issue: Temperature Abuse: Product exposed to temperature outside specified limits.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugApril 28, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: DELFLEX Peritoneal Dialysis Solution with 2.5% Dextrose Recalled by...

The Issue: Temperature Abuse: Product exposed to temperature outside specified limits.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugApril 28, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: DELFLEX Peritoneal Dialysis Solution with 1.5% Dextrose Recalled by...

The Issue: Temperature Abuse: Product exposed to temperature outside specified limits.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugApril 28, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: DELFLEX Peritoneal Dialysis Solution with 1.5% Dextrose Recalled by...

The Issue: Temperature Abuse: Product exposed to temperature outside specified limits.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugApril 28, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: DELFLEX Peritoneal Dialysis Solution with 1.5% Dextrose Recalled by...

The Issue: Temperature Abuse: Product exposed to temperature outside specified limits.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
FoodApril 28, 2021· NOW Health Group Inc.

Recalled Item: NOW 4x6 Acidophilus Recalled by NOW Health Group Inc. Due to Undeclared...

The Issue: Foreign capsules included in bottle. Undeclared ingredients.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
Medical DeviceApril 28, 2021· Randox Laboratories Ltd.

Recalled Item: Randox RX Imola Analyser with ISE Recalled by Randox Laboratories Ltd. Due...

The Issue: An issue was identified where the software froze during processing of...

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

Class II — Potential Health HazardOngoing