Product Recalls in Ohio
Product recalls affecting Ohio — including food, drugs, consumer products, medical devices, and vehicles distributed to Ohio. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,072 recalls have been distributed to Ohio in the last 12 months.
Showing 18621–18640 of 55,415 recalls
Recalled Item: OSTEORAPTOR CRVD 2.3 SA UB COBRD BLUE- Absorbable Suture anchor Recalled by...
The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICRORAPTOR REGENESORB SUTURE ANCHOR- Absorbable Suture anchor Product...
The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEALICOIL RSB SA 5.5MM W/1 UT & 1 UB BLK- Recalled by Smith & Nephew, Inc....
The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEORAPTOR 2.9 W/ 1 UB COBRAID BLUE -Absorbable Suture anchor Recalled by...
The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX ULTRA PLLA/HA 5.5 W/3 UB-Absorbable Suture anchor Product Number:...
The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX ULTRA HA 5.5 W/2 UB BLUE & BLK- Absorbable Recalled by Smith &...
The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RAPTORMITE 3.7MM AB W/ NEEDLES AND TWO-Absorbable Suture anchor Product...
The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEORAPTOR CRVD 2.3 SA UB COBRD BLACK- Absorbable Suture anchor Recalled by...
The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Buttered microwave popcorn packaged in the following ways: 1) Full Recalled...
The Issue: Popcorn ingredient was recalled due to foreign matter: tempered glass...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Microwave popcorn packaged in the following ways: 1) Full Circle Recalled by...
The Issue: Popcorn ingredient was recalled due to foreign matter: tempered glass...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lightly salted microwave popcorn packaged in the following ways: 1) Recalled...
The Issue: Popcorn ingredient was recalled due to foreign matter: tempered glass...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Light microwave popcorn packaged in the following ways: 1) Full Recalled by...
The Issue: Popcorn ingredient was recalled due to foreign matter: tempered glass...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cadia Organic Unsalted Microwave Popcorn Recalled by Gilster-Mary Lee Corp....
The Issue: Popcorn ingredient was recalled due to foreign matter: tempered glass...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: AESCULAP S4 Cervical Cross Connector L 33-42mm Recalled by Aesculap Implant...
The Issue: Insufficient clamping force of the cross connectors in the spinal surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AESCULAP S4 Cervical Cross Connector L24mm Recalled by Aesculap Implant...
The Issue: Insufficient clamping force of the cross connectors in the spinal surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AESCULAP S4 Cervical Cross Connector L 42-58mm Recalled by Aesculap Implant...
The Issue: Insufficient clamping force of the cross connectors in the spinal surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AESCULAP S4 Cervical Cross Connector Recalled by Aesculap Implant Systems...
The Issue: Insufficient clamping force of the cross connectors in the spinal surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AESCULAP S4 Cervical Cross Connector L22mm Recalled by Aesculap Implant...
The Issue: Insufficient clamping force of the cross connectors in the spinal surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AESCULAP S4 Cervical Cross Connector L 28-33mm Recalled by Aesculap Implant...
The Issue: Insufficient clamping force of the cross connectors in the spinal surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Recalled by GE Healthcare, LLC Due to Potential electrical arc flash...
The Issue: Potential electrical arc flash within the Power Gradient & RF (PGR) Cabinet.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.