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. 2,489 recalls have been distributed to Rhode Island in the last 12 months.
Showing 13541–13560 of 47,970 recalls
Recalled Item: Old Spice Recalled by The Procter & Gamble Company Due to CGMP Deviation;...
The Issue: CGMP Deviation; manufactured at the same facility where other lots were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Secret Recalled by The Procter & Gamble Company Due to Chemical...
The Issue: Chemical contamination: presence of benzene
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Secret Dry Spray Recalled by The Procter & Gamble Company Due to CGMP...
The Issue: CGMP Deviation; manufactured at the same facility where other lots were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Secret Recalled by The Procter & Gamble Company Due to CGMP Deviation;...
The Issue: CGMP Deviation; manufactured at the same facility where other lots were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Old Spice Recalled by The Procter & Gamble Company Due to Chemical...
The Issue: Chemical contamination: presence of benzene
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Secret Recalled by The Procter & Gamble Company Due to Chemical...
The Issue: Chemical contamination: presence of benzene
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Secret Recalled by The Procter & Gamble Company Due to CGMP Deviation;...
The Issue: CGMP Deviation; manufactured at the same facility where other lots were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Secret Recalled by The Procter & Gamble Company Due to CGMP Deviation;...
The Issue: CGMP Deviation; manufactured at the same facility where other lots were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 1. Sensis Recalled by Siemens Medical Solutions USA, Inc Due to Software...
The Issue: Software error which affects Sensis Vibe Hemo, Sensis and Sensis Vibe Combo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BALLARD* Multi-Access Port Catheter Recalled by Avanos Medical, Inc. Due to...
The Issue: Product was distributed with incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BALLARD* Multi-Access Port (MAP) Catheter Recalled by Avanos Medical, Inc....
The Issue: Product was distributed with incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BALLARD* Seal Cassette Replacement MAP - BALLARD* Seal Cassette Replacement...
The Issue: Product was distributed with incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products High Sample Diluent A Reagent Pack Recalled...
The Issue: Lower than expected results for VITROS¿ Immunodiagnostic Products TSH...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electri-Cool II Portable Cold Therapy Unit Recalled by Gentherm Medical, LLC...
The Issue: This recall has been initiated to provide a labeling update with revised...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UROMEDICA Implantation Instrument Set (Sheath and Sharp Trocar) Recalled by...
The Issue: The U-channel sheaths may cause damage to ProACT implant devices when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ripple Dairy-Free. As It Should Be 8g Plant Based Protein Recalled by RIPPLE...
The Issue: Complaint led investigation found the presence of Bacillus Cereus in one lot...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Hydrocodone Bitartrate and Acetaminophen Tablets Recalled by Ascent...
The Issue: Product Mix-up
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AmericanScreening HAND SANITIZER (ethyl alcohol 70%) ANTIMICROBIAL FORMULA...
The Issue: Labeling Not Elsewhere Classified: Hand sanitizer packaged in containers...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tydemy (drospirenone Recalled by Lupin Pharmaceuticals Inc. Due to Subpotent...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Birds Eye Broccoli Tots Recalled by CONAGRA BRANDS Due to Small rocks and...
The Issue: Small rocks and metal fragments in the product
Recommended Action: Do not consume. Return to store for a refund or discard.