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. 2,592 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,592 in last 12 months

Showing 1442114440 of 49,976 recalls

Medical DeviceOctober 1, 2021· Cordis Corporation

Recalled Item: SMART FLEX 10x100 BIL Recalled by Cordis Corporation Due to There is a...

The Issue: There is a potential for distal tip dislodgement or separation.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2021· Cordis Corporation

Recalled Item: SMART FLEX 10x100 BIL Recalled by Cordis Corporation Due to There is a...

The Issue: There is a potential for distal tip dislodgement or separation.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2021· Cordis Corporation

Recalled Item: SMART FLEX 8x60 BIL Recalled by Cordis Corporation Due to There is a...

The Issue: There is a potential for distal tip dislodgement or separation.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2021· Cordis Corporation

Recalled Item: SMART FLEX 9x60 BIL Recalled by Cordis Corporation Due to There is a...

The Issue: There is a potential for distal tip dislodgement or separation.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2021· Cordis Corporation

Recalled Item: SMART FLEX 6x120 BIL Recalled by Cordis Corporation Due to There is a...

The Issue: There is a potential for distal tip dislodgement or separation.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2021· Limacorporate S.p.A

Recalled Item: .15.020 Recalled by Limacorporate S.p.A Due to There is a potential that the...

The Issue: There is a potential that the length of bone screws identified on labeling...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2021· Limacorporate S.p.A

Recalled Item: .15.010 Recalled by Limacorporate S.p.A Due to There is a potential that the...

The Issue: There is a potential that the length of bone screws identified on labeling...

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

Class II — Potential Health HazardOngoing
DrugSeptember 30, 2021· Beiersdorf Inc

Recalled Item: Coppertone Pure & Simple kids 50 Sunscreen Spray (To Deliver) Zinc Oxide...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 30, 2021· Beiersdorf Inc

Recalled Item: Coppertone SPORT MINERAL 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%...

The Issue: Chemical contamination; presence of benzene

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 30, 2021· Beiersdorf Inc

Recalled Item: Coppertone Pure & Simple 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 30, 2021· Beiersdorf Inc

Recalled Item: Coppertone Pure & Simple kids 50 Sunscreen Spray (To Deliver) Zinc Oxide...

The Issue: Chemical contamination; presence of benzene

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 30, 2021· Beiersdorf Inc

Recalled Item: Coppertone SPORT Sunscreen Spray 50 Recalled by Beiersdorf Inc Due to...

The Issue: Chemical contamination; presence of benzene

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 30, 2021· Beiersdorf Inc

Recalled Item: Coppertone Pure & Simple baby 50 Sunscreen Spray (To Deliver) Zinc Oxide...

The Issue: Chemical contamination; presence of benzene

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 30, 2021· Beiersdorf Inc

Recalled Item: Coppertone Pure & Simple baby 50 Sunscreen Spray (To Deliver) Zinc Oxide...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 30, 2021· Beiersdorf Inc

Recalled Item: Coppertone Pure & Simple 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%...

The Issue: Chemical contamination; presence of benzene

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 30, 2021· Mentor Texas, LP.

Recalled Item: MENTOR Saline-Filled Breast Implants are constructed from room temperature...

The Issue: Due to a manufacturing issue, Implant may have a potentially weakened area...

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

Class II — Potential Health HazardOngoing
FoodSeptember 29, 2021· B&G Foods North America, Inc

Recalled Item: Tone s Taco Seasoning Blend Recalled by B&G Foods North America, Inc Due to...

The Issue: Product was recalled due to the presence of undeclared wheat.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 29, 2021· Abbott Laboratories

Recalled Item: ARCHITECT i1000SR /1L86 and 1L87 Recalled by Abbott Laboratories Due to...

The Issue: Twelve software-related issues affecting software version 9.41 and earlier...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2021· Abbott Laboratories

Recalled Item: ARCHITECT c4000 /2P24 Recalled by Abbott Laboratories Due to Twelve...

The Issue: Twelve software-related issues affecting software version 9.41 and earlier...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2021· CooperSurgical, Inc.

Recalled Item: Quantum 2000 Electrosurgical Generators Cooper Surgical Part Number: 909075...

The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...

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

Class II — Potential Health HazardOngoing