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. 2,457 recalls have been distributed to Rhode Island in the last 12 months.
Showing 14541–14560 of 27,456 recalls
Recalled Item: TriMed Hex Driver 1.2 Recalled by TriMed Inc. Due to The epoxy on Apex...
The Issue: The epoxy on Apex manufactured epoxy-coated instruments can pop off.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriMed Locking Drill Guide Recalled by TriMed Inc. Due to The epoxy on Apex...
The Issue: The epoxy on Apex manufactured epoxy-coated instruments can pop off.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriMed Countersink 1.7mm Recalled by TriMed Inc. Due to The epoxy on Apex...
The Issue: The epoxy on Apex manufactured epoxy-coated instruments can pop off.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriMed Wrist Hook Dorsal Impactor Recalled by TriMed Inc. Due to The WHD/WHV...
The Issue: The WHD/WHV impactors can rust over time due to an improper manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aisys CS2 Anesthesia System. Sold under the following product names: AISYS...
The Issue: Upgraded Aisys anesthesia devices and Aisys CS2 anesthesia devices with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Touchscreen display kit. Sold under the following product names: TOUCHSCREEN...
The Issue: Upgraded Aisys anesthesia devices and Aisys CS2 anesthesia devices with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aisys Anesthesia System. Sold under the following product names: AISYS...
The Issue: Upgraded Aisys anesthesia devices and Aisys CS2 anesthesia devices with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer: In vitro diagnostic testing of clinical Recalled...
The Issue: Multiple Issues Identified in Atellica Solution System Software in V 1.14.2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TB Series Bipolar Pacing Leads Recalled by Oscor, Inc. Due to During the use...
The Issue: During the use of some TB - Temporary Bipolar Pacing Leads, featuring the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCEA ASV Yellow Microbore Recalled by Becton Dickinson & Company Due to The...
The Issue: The products have the potential to leak between the connection of the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH 930 Analyzer. In vitro diagnostic testing of clinical Recalled...
The Issue: Multiple Issues Identified in Atellica Solution System Software in V 1.14.2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCEA Kit ASV Yellow Stripe Microbore Recalled by Becton Dickinson & Company...
The Issue: The products have the potential to leak between the connection of the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1300 Analyzer. In vitro diagnostic testing of clinical Recalled...
The Issue: Multiple Issues Identified in Atellica Solution System Software in V 1.14.2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica Sample Handler Prime. In vitro diagnostic testing of clinical...
The Issue: Multiple Issues Identified in Atellica Solution System Software in V 1.14.2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zilver 518 Biliary Stent 5mm x 30mm Recalled by Cook Medical Incorporated...
The Issue: The instruction for use detail, with respect to removal of the delivery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giraffe Incubator Carestation. Neonatal incubator. Device sold under the...
The Issue: Potential electric leakage affecting the user.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panda Freestanding Warmer. Device sold under the following product names:...
The Issue: Potential electric leakage affecting the user.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giraffe OmniBed Carestation. Neonatal incubator. Device sold under the...
The Issue: Potential electric leakage affecting the user.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giraffe Warmer. Device sold under the following product names: Giraffe...
The Issue: Potential electric leakage affecting the user.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panda iRes Infant Radiant Warmer. Device sold under the following Recalled...
The Issue: Potential electric leakage affecting the user.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.