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. 2,276 recalls have been distributed to Rhode Island in the last 12 months.
Showing 43081–43100 of 47,970 recalls
Recalled Item: Maalox Regular Strength Antacid (calcium carbonate) chewable tablets...
The Issue: Labeling: Incorrect Or Missing Lot and/or Exp Date: The lot number and/or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Maalox Advanced Maximum Strength Antacid & Antigas (calcium carbonate and...
The Issue: Labeling: Incorrect Or Missing Lot and/or Exp Date: The lot number and/or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Maalox Extra Strength Antacid with Anti-Gas (calcium carbonate and...
The Issue: Labeling: Incorrect Or Missing Lot and/or Exp Date: The lot number and/or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: REEVA (triclosan) Antibacterial Hand Soap and Dishwashing Liquid Recalled by...
The Issue: Microbial Contamination of a Non-Sterile Products: Product was found to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Maalox Advanced Maximum Strength Antacid & Antigas (calcium carbonate and...
The Issue: Labeling: Incorrect Or Missing Lot and/or Exp Date: The lot number and/or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Benefiber Recalled by Novartis Consumer Health Due to The lot number and/or...
The Issue: The lot number and/or expiration date may be illegible on the outer plastic...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Benefiber Recalled by Novartis Consumer Health Due to The lot number and/or...
The Issue: The lot number and/or expiration date may be illegible on the outer plastic...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Benefiber Recalled by Novartis Consumer Health Due to The lot number and/or...
The Issue: The lot number and/or expiration date may be illegible on the outer plastic...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Benefibre Recalled by Novartis Consumer Health Due to The lot number and/or...
The Issue: The lot number and/or expiration date may be illegible on the outer plastic...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Benefiber Recalled by Novartis Consumer Health Due to The lot number and/or...
The Issue: The lot number and/or expiration date may be illegible on the outer plastic...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: OSTEORAPTOR 2.3 mm Suture Anchor with 1 ULTRABRAID COBRAID Suture Recalled...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEORAPTOR 2.9 mm Suture Anchor with 2 ULTRABRAID Suture Recalled by Smith...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEORAPTOR 2.9 mm Suture Anchor with 1 ULTRABRAID Suture Recalled by Smith...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIORAPTOR 2.9 mm Suture Anchor Straight Recalled by Smith & Nephew, Inc....
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX Ultra 5.5 mm PLLA-HA Suture Anchor with two #2 ULTRABRAID Sutures...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEORAPTOR 2.9 mm Suture Anchor with 2 ULTRABRAID Suture Recalled by Smith...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEORAPTOR CURVED 2.3 mm Suture Anchor SA ULTRABRAID COBRAID Suture...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX" Ultra PLLA/HA 6.5 mm with 2 ULTRABRAID" Suture Recalled by Smith &...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTOSTEORAPTOR 2.9 mm Suture Anchor with 1 ULTRABRAID COBRAID Suture...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX ULTRA PLLA/HA 5.5 mm Suture Anchor with 3 ULTRABRAID Recalled by...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.