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. 2,363 recalls have been distributed to Rhode Island in the last 12 months.
Showing 25161–25180 of 47,970 recalls
Recalled Item: Vulcan Fast Red Chromogen Kit 2 Recalled by Biocare Medical, LLC Due to...
The Issue: Chromogen failed to develop due to a stability issue caused by environmental...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE O.R. Necessities(R) STERILE R Recalled by Medline Industries Inc Due...
The Issue: The product packaging seal has the potential to experience seal creep. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE O.R. Necessities(TM) Sterile* Needle Counter Recalled by Medline...
The Issue: The product packaging seal has the potential to experience seal creep. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE O.R. Necessities(TM) Sterile* Needle Counter Recalled by Medline...
The Issue: The product packaging seal has the potential to experience seal creep. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE Sterile* Needle Counter Recalled by Medline Industries Inc Due to...
The Issue: The product packaging seal has the potential to experience seal creep. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE Sterile* Needle Counter Recalled by Medline Industries Inc Due to...
The Issue: The product packaging seal has the potential to experience seal creep. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lean Pro 8 Vanilla 2 Recalled by Labrada Nutrition, Inc Due to Undeclared Egg
The Issue: Undeclared egg
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lean Pro 8 Chocolate 2 Recalled by Labrada Nutrition, Inc Due to Undeclared Egg
The Issue: Undeclared egg
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lean Pro 8 Cookies & Cream 1 Recalled by Labrada Nutrition, Inc Due to...
The Issue: Undeclared egg
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Diltiazem HCl Extended-Release Capsules Recalled by Mckesson Packaging...
The Issue: Failed Dissolution Specifications. High dissolution results were obtained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diltiazem HCl Extended-Release Capsules Recalled by Mckesson Packaging...
The Issue: Failed Dissolution Specifications. High dissolution results were obtained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Dr. Reddy's...
The Issue: Presence of Foreign Tablets/Capsules: One foreign tablet identified as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diltiazem CD (Diltiazem Hydrochloride Extended-Release Capsules Recalled by...
The Issue: Failed Dissolution Specifications. High dissolution results were obtained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diclofenac Sodium and Misoprostol Delayed Release Tablets 75 mg/0.2 mg...
The Issue: Labeling: Label Mix-Up: bottle labeled as Diclofenac Sodium and Misoprostol...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LINX Management System Recalled by Torax Medical, Inc. Due to Possible out...
The Issue: Possible out of specification condition which may allow a bead component to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINX Management System Recalled by Torax Medical, Inc. Due to Possible out...
The Issue: Possible out of specification condition which may allow a bead component to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINX Management System Recalled by Torax Medical, Inc. Due to Possible out...
The Issue: Possible out of specification condition which may allow a bead component to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.Now Recalled by Siemens Medical Solutions USA, Inc Due to There...
The Issue: There is a potential for a software issue that may cause the need for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINX Management System Recalled by Torax Medical, Inc. Due to Possible out...
The Issue: Possible out of specification condition which may allow a bead component to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Infusion Pump administration sets labeled as: -Infusion Set Alaris...
The Issue: Complaints where users were unable to prime the administration set.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.