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. 2,351 recalls have been distributed to Rhode Island in the last 12 months.
Showing 25521–25540 of 27,456 recalls
Recalled Item: Stryker Irrigator Reusable Tips: 3mm X 32cm Regular Tip Recalled by Stryker...
The Issue: The pre-vacuum steam sterilization (wrapped method) temperature in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Irrigator Reusable Tips: 5mm X 28cm Regular Tip Recalled by Stryker...
The Issue: The pre-vacuum steam sterilization (wrapped method) temperature in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Crimpers Recalled by Edwards Lifesciences, LLC Due to...
The Issue: Holes in the sterile barrier pouch may be caused by handling of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Recalled by GE Healthcare, LLC Due to GE Healthcare has recently become...
The Issue: GE Healthcare has recently become aware of a potential safety issue related...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varian brand RPM Respiratory Gating System Recalled by Varian Medical...
The Issue: Varian has identified an anomaly with the RPM Respiratory Gating System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE PET Discovery 610 Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a potential safety issue related...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Crimpers Recalled by Edwards Lifesciences, LLC Due to...
The Issue: Holes in the sterile barrier pouch may be caused by handling of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediChoice¿ Rayon Tipped OB/GYN Applicator Recalled by Owens & Minor...
The Issue: Owens & Minor Distribution, Inc. is conducting a market withdrawal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Antimicrobial Susceptibility Test Discs F300 (Nitrofurantoin) Recalled...
The Issue: Use of affected lots may give false indication of susceptibility to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Triathlon Femoral Distal Augment- Left Recalled by...
The Issue: Stryker Orthopaedics received a report that a label on the external...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KWIK-STIK(TM) Recalled by Microbiologics Inc Due to Some of the KWIK-STIK...
The Issue: Some of the KWIK-STIK Catalog #01023P Campylobacter coli, Lot# 1023-05-7,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...
The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed Paradigm Insulin Infusion Pumps Model Numbers: MMT-511...
The Issue: Medtronic is recalling the Medtronic Paradigm Insulin Pump because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...
The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOCORD One Violet and One Blue Braided Composite Suture with Recalled by...
The Issue: The IFU provided with the free strand ORTHOCORD sutures currently indicates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...
The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...
The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOCORD ONE VIOLET AND ONE BLUE BRAIDED COMPOSITE SUTURE 2 (5 METRIC)...
The Issue: The IFU provided with the free strand ORTHOCORD sutures currently indicates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOCORD One Violet and One Blue Braided Composite Suture with Recalled by...
The Issue: The IFU provided with the free strand ORTHOCORD sutures currently indicates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD 200 Sterilization System Recalled by Advanced Sterilization Products...
The Issue: The recall was initiated because Advanced Sterilization Products (ASP) has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.