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. 2,539 recalls have been distributed to Rhode Island in the last 12 months.
Showing 4501–4520 of 47,970 recalls
Recalled Item: Biodesign Fistula Plug C-FPS-0.7 - For implantation to reinforce soft...
The Issue: Products expire prior to the expiration date printed on the product labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthroscopy Pack Recalled by American Contract Systems, Inc. Due to ACS...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biodesign Fistula Plug C-FPS-0.4 - For implantation to reinforce soft...
The Issue: Products expire prior to the expiration date printed on the product labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Open Shoulder Recalled by American Contract Systems, Inc. Due to ACS...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biodesign Fistula Plug C-FPB-0.7 - For implantation to reinforce soft...
The Issue: Products expire prior to the expiration date printed on the product labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FILMARRAY TORCH MODULE BOX Recalled by BioFire Diagnostics, LLC Due to...
The Issue: Some automated in vitro diagnostic modules and instruments manufactured or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PACEMAKER PACK Recalled by American Contract Systems, Inc. Due to ACS...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neuro Vascular Recalled by American Contract Systems, Inc. Due to ACS...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion 7M20 systems with FlexArm ceiling-mounted system Recalled by...
The Issue: The motorized longitudinal movement of the FlexArm stand may be inconsistent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: General Purpose Syringe McKesson 60 mL Luer Lock Tip Without Safety Recalled...
The Issue: The syringes that were inadvertently shipped from the Distribution Center....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IBU Ibuprofen Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Failed impurities/degradation specifications: results for unknown impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IBU Ibuprofen Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Failed impurities/degradation specifications: results for unknown impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IBU Ibuprofen Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Failed impurities/degradation specifications: results for unknown impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CVS Health brand and HEB Baby brand Premium Infant Formula Recalled by PBM...
The Issue: Product contains levels of Vitamin D above the maximum level permitted.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HAND-I-SAN Recalled by Zeco LLC Due to CGMP Deviations: sterile water not...
The Issue: CGMP Deviations: sterile water not used for production
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rubbing Alcohol (70% Isopropyl Alcohol) Recalled by Zeco LLC Due to CGMP...
The Issue: CGMP Deviations: sterile water not used for production
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ERIC Retrieval Device ER174030 ER176044 The ERIC Retrieval Recalled by...
The Issue: Due to Retrieval Device product labels stating the incorrect expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella CP Pump 371 Set Recalled by Abiomed, Inc. Due to A potential device...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella 5.5 SmartAssist S2 Set Recalled by Abiomed, Inc. Due to A potential...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella CP Smart Assist Set APAC Recalled by Abiomed, Inc. Due to A...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.