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. 2,314 recalls have been distributed to Rhode Island in the last 12 months.
Showing 39801–39820 of 47,970 recalls
Recalled Item: Welchol Tablets (colesevelam HCl) 625 mg Recalled by Daiichi Sankyo Pharma...
The Issue: Temperature Abuse; various products were not stored at Controlled Room...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Benicar HCT Tablets (olmesartan medoxomil/hydrochlorothiazide) 40 mg/12.5 mg...
The Issue: Temperature Abuse; various products were not stored at Controlled Room...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets Recalled by Jubilant...
The Issue: Presence of Foreign Substance: Tablets may contain dark blemishes identified...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Baxter Healthcare Corp. Due...
The Issue: Presence of Particulate Matter: particulate matter identified as fibers...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Orphenadrine Citrate Extended Release Tablets Recalled by Sandoz Inc Due to...
The Issue: Failed Dissolution Specifications: Product found to be out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection USP MINI-BAG Plus Container Recalled by...
The Issue: Presence of Particulate Matter: particulate matter identified as fibers...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...
The Issue: Presence of Particulate Matter: particulate matter identified as fibers...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medtronic Ascenda Intrathecal Catheter models 8780 and 8781 Recalled by...
The Issue: Medtronic is removing specific lots of the Ascenda Intrathecal Catheters and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlowCOUPLER. An implantable device that is used to detect blood Recalled by...
The Issue: Baxter Healthcare is recalling the FlowCOUPLER Device because there is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibila Insert UC Recalled by Ortho Development Corporation Due to Ortho...
The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amerigel Wound Dressing Maximum Strength CAT# A2001. Wound management....
The Issue: Not approved labeling claims (antimicrobial and autolytic debridement)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amerigel Post-Op Surgical Kits . Kit includes: Amerigel Wound Dressing...
The Issue: Not approved labeling claims (antimicrobial and autolytic debridement)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PS Tibial Insert Recalled by Ortho Development Corporation Due to Ortho...
The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amerigel Hydrogel Saturated Gauze Dressing Recalled by Amerx Health Care...
The Issue: Not approved labeling claims (antimicrobial and autolytic debridement)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Patella 38mm Recalled by Ortho Development Corporation Due to Ortho...
The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amerigel Daily Dressing Advanced 3-in-1 Hydrogel Recalled by Amerx Health...
The Issue: Not approved labeling claims (antimicrobial and autolytic debridement)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pivot Bipolar Cup 22x42/43-51/53mm Recalled by Ortho Development Corporation...
The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibila Insert CK Recalled by Ortho Development Corporation Due to Ortho...
The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Positioning Rapid Response HUT table Recalled by Medical Positioning...
The Issue: Excessive weight on the table will cause tables with the affected component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Positioning Rapid Response HUT table Recalled by Medical Positioning...
The Issue: Excessive weight on the table will cause tables with the affected component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.