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. 1,042 recalls have been distributed to Rhode Island in the last 12 months.
Showing 13601–13620 of 27,456 recalls
Recalled Item: Arrow¿ PICC with Chlorag+ard¿ Technology Product Code: PR 45552 HPHNL...
The Issue: Lidstock states the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow PICC with Chlorag+ard Technology Product Code: CDA 45552 VPS2 Recalled...
The Issue: Lidstock states the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow¿ PICC with Chlorag+ard Technology Product Code:PR 45541 HPHNM Recalled...
The Issue: Lidstock states the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow¿ JACC with Chlorag+ard¿ Technology Jugular Axillo subclavian Central...
The Issue: Lidstock states the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrowg+ard Blue Advance JACC Product Code: CDC 41552 JX1A Recalled by Arrow...
The Issue: Lidstock states the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow PICC with Chlorag+ard Technology Product Code: CDA 45541 HPK1A...
The Issue: Lidstock states the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrowg+ard Blue Advance Midline Product Code: PR 41541 BAS Recalled by Arrow...
The Issue: Lidstock states the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrowg+ard Blue Advance JACC Product Code: CDC 42041 JX1A Recalled by Arrow...
The Issue: Lidstock states the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow¿ JACC with Chlorag+ard Technology Product Code: JR 42041 HPHNM...
The Issue: Lidstock states the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrowg+ard Blue Advance PICC Product Code: CDC45541HPK1A Recalled by Arrow...
The Issue: Lidstock states the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEEP Precision Integrated System 120V Recalled by CooperSurgical, Inc. Due...
The Issue: 2.5A slow blow fuses may have been installed in the LEEP RPECISION Generator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow PICC Kit Product Code: ASK 45541 RWJ4 Recalled by Arrow International...
The Issue: Lidstock states the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cook Kwart Retro-Inject Ureteral Stent Set: PRODUCT/CATALOG NUMBER/GPN: 4.7...
The Issue: Kwart RetroInject Stent Set (Multi-Length) and Salle Intraoperative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cook Salle Intraoperative Pyeloplasty Stent Set PRODUCT/CATALOG NUMBER/GPN:...
The Issue: Kwart RetroInject Stent Set (Multi-Length) and Salle Intraoperative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETHIBOND EXCEL ETHIBOND Polvester Suture-Green 75cm USP1 Single Armed CTX...
The Issue: Possibility that a suture raw material containing high endotoxin levels was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.