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. 2,517 recalls have been distributed to Rhode Island in the last 12 months.
Showing 9601–9620 of 47,970 recalls
Recalled Item: Gabapentin Tablets Recalled by Sciegen Pharmaceuticals Inc Due to Presence...
The Issue: Presence of Foreign Tablets/Capsules: Pharmacist reported presence of some...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Stainless Steel Water Bottle The product comes in four sizes: 32 oz....
The Issue: Water bottle has a cup with a screw cap attached by a weld that has been...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Agilent Resolution ctDx FIRST Sample Collection Kit Recalled by AGILENT...
The Issue: Distributed sample collection kit with an unapproved instruction for use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Raystation treatment planning system for radiation therapy Recalled by...
The Issue: It is possible to set a non-zero collimator angle in the Virtual Simulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...
The Issue: Incorrect type of titanium was used which reduces the gripping strength of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...
The Issue: Incorrect type of titanium was used which reduces the gripping strength of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...
The Issue: Incorrect type of titanium was used which reduces the gripping strength of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...
The Issue: Incorrect type of titanium was used which reduces the gripping strength of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...
The Issue: Incorrect type of titanium was used which reduces the gripping strength of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Testosterone Cypionate Injection Recalled by Azurity Pharmaceuticals, Inc....
The Issue: cGMP: complaints of crystals not redissolving into solution after warming...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Buprenorphine Transdermal System Recalled by AVEVA Drug Delivery Systems,...
The Issue: Failed Impurities/Degradation Specifications: Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Buprenorphine Transdermal System Recalled by AVEVA Drug Delivery Systems,...
The Issue: Failed Impurities/Degradation Specifications: Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Warfarin Sodium Tablets Recalled by RISING PHARMACEUTICALS Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FoundationOne Companion Diagnostic (F1CDx) Recalled by Foundation Medicine,...
The Issue: An incorrect negative claim was identified on the claims page; the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flex-Neck Catheter External Repair Kit LOT CE-1400/A Recalled by Merit...
The Issue: Product that was built for design verification testing was inadvertently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Attune Revision Limb Preservation System (LPS) Tibial Insert XXSM 18MM...
The Issue: The subject product lots are being recalled because they received a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Attune Revision Limb Preservation System (LPS) Tibial Insert SM 12MM...
The Issue: The subject product lots are being recalled because they received a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Attune Revision Limb Preservation System (LPS) Tibial Insert XSM 12MM...
The Issue: The subject product lots are being recalled because they received a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Attune Revision Limb Preservation System (LPS) Tibial Insert XSM 26MM...
The Issue: The subject product lots are being recalled because they received a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Attune Posterior (PS) Fixed Bearing (FB) Tibial Insert SZ5 7MM Recalled by...
The Issue: The subject product lots are being recalled because they received a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.