Product Recalls in Rhode Island
Product recalls affecting Rhode Island — including food, drugs, consumer products, medical devices, and vehicles distributed to Rhode Island. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,401 recalls have been distributed to Rhode Island in the last 12 months.
Showing 18161–18180 of 27,456 recalls
Recalled Item: IQon Spectral CT with software version 4.7.0 Product Usage: The Recalled by...
The Issue: Multiple issues have caused the device to result in CT rescans or incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST Fosfomycin FM1024 Blister packaging Recalled by BioMerieux SA Due to...
The Issue: Product Stability issues: The current shelf-life claims of the ETEST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST Ceftriaxone TXL32 FOAM packaging Recalled by BioMerieux SA Due to...
The Issue: Product Stability issues: The current shelf-life claims of the ETEST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST Tobramycin TM256 FOAM packaging Recalled by BioMerieux SA Due to...
The Issue: Product Stability issues: The current shelf-life claims of the ETEST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ciprofloxacin CI 32 Foam packaging Recalled by BioMerieux SA Due to Product...
The Issue: Product Stability issues: The current shelf-life claims of the ETEST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST Ceftazidime TZ256 Foam packaging Recalled by BioMerieux SA Due to...
The Issue: Product Stability issues: The current shelf-life claims of the ETEST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST Doripenem DOR32 FOAM packaging Recalled by BioMerieux SA Due to...
The Issue: Product Stability issues: The current shelf-life claims of the ETEST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST Cephalotin CE 256 Foam packaging Recalled by BioMerieux SA Due to...
The Issue: Product Stability issues: The current shelf-life claims of the ETEST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST Gentamicin GM256 FOAM packaging Recalled by BioMerieux SA Due to...
The Issue: Product Stability issues: The current shelf-life claims of the ETEST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST¿ Ceftriaxone TXL32 SPB Recalled by BioMerieux SA Due to Product...
The Issue: Product Stability issues: The current shelf-life claims of the ETEST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST Imipenem IP32 Foam packaging Recalled by BioMerieux SA Due to Product...
The Issue: Product Stability issues: The current shelf-life claims of the ETEST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST Vancomycin VA 256 FOAM packaging Recalled by BioMerieux SA Due to...
The Issue: Product Stability issues: The current shelf-life claims of the ETEST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST Benzyl Penicillin PG256 FOAM packaging Recalled by BioMerieux SA Due...
The Issue: Product Stability issues: The current shelf-life claims of the ETEST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NanoTips 30g 20pk Recalled by Ultradent Products, Inc. Due to Ultradent...
The Issue: Ultradent Products, Inc. announces a voluntary field action for the NanoTips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPS-1 Recalled by Organ Recovery Systems, Inc. Due to Organ preservation...
The Issue: Organ preservation fluid recalled due to potential for bacterial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 16 mm [or 18 mm] Distraction Pin Recalled by MEDLINE INDUSTRIES INC Due to...
The Issue: Product's non-conformity involves the integrity of the seal in the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10 mm Distraction Pin Recalled by MEDLINE INDUSTRIES INC Due to Product's...
The Issue: Product's non-conformity involves the integrity of the seal in the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 16 mm Distraction Pin Recalled by MEDLINE INDUSTRIES INC Due to Product's...
The Issue: Product's non-conformity involves the integrity of the seal in the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 12 mm Distraction Pin Recalled by MEDLINE INDUSTRIES INC Due to Product's...
The Issue: Product's non-conformity involves the integrity of the seal in the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 14 mm Distraction Pin Recalled by MEDLINE INDUSTRIES INC Due to Product's...
The Issue: Product's non-conformity involves the integrity of the seal in the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.