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. 2,521 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,521 in last 12 months

Showing 87018720 of 27,456 recalls

Medical DeviceNovember 2, 2021· Cardinal Health

Recalled Item: RoyalSilk Non-Reinforced Surgical Gowns XX-large SKU: 9578 Recalled by...

The Issue: Potential for open packaging seals compromising the sterility of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2021· Cardinal Health

Recalled Item: Cardinal Health Poly-Reinforced Surgical Gowns XX-large SKU: 9070 Recalled...

The Issue: Potential for open packaging seals compromising the sterility of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2021· Cardinal Health

Recalled Item: SmartGown Breathable Surgical Gowns with raglan sleeves X-large Recalled by...

The Issue: Potential for open packaging seals compromising the sterility of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2021· Cardinal Health

Recalled Item: Cardinal Health Poly-Reinforced Surgical Gowns X-large SKU: 9040 Recalled by...

The Issue: Potential for open packaging seals compromising the sterility of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2021· Cardinal Health

Recalled Item: RoyalSilk Non-Reinforced Surgical Gowns XXX-large Recalled by Cardinal...

The Issue: Potential for open packaging seals compromising the sterility of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2021· Magnolia Medical Technologies, Inc.

Recalled Item: The Steripath Gen2 Blood Collection System Model Number/Description...

The Issue: Due to an uptick of complaints associated with premature needle retraction...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2021· Human Care USA, Inc.

Recalled Item: Hanger-Bar 2P 45cm Recalled by Human Care USA, Inc. Due to The Hanger-Bar is...

The Issue: The Hanger-Bar is being recalled due to the potential for the set screw...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2021· Human Care USA, Inc.

Recalled Item: Hanger-Bar 2P 45cm Recalled by Human Care USA, Inc. Due to The Hanger-Bar is...

The Issue: The Hanger-Bar is being recalled due to the potential for the set screw...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2021· Smith & Nephew, Inc.

Recalled Item: smith&Nephew EVOS MEDIAL DISTAL FEMUR PLATE Recalled by Smith & Nephew, Inc....

The Issue: Testing vendor notified Smith & Nephew that previous MRI scanning conditions...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2021· Smith & Nephew, Inc.

Recalled Item: smith&nephew EVOS CONDYLAR MEDIAL DISTAL FEMUR PLATE Recalled by Smith &...

The Issue: Testing vendor notified Smith & Nephew that previous MRI scanning conditions...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2021· Smith & Nephew, Inc.

Recalled Item: smith&nephew EVOS CONDYLAR MEDIAL DISTAL FEMUR PLATE Recalled by Smith &...

The Issue: Testing vendor notified Smith & Nephew that previous MRI scanning conditions...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2021· Smith & Nephew, Inc.

Recalled Item: smith&nephew EVOS MEDIAL DISTAL FEMUR PLATE Recalled by Smith & Nephew, Inc....

The Issue: Testing vendor notified Smith & Nephew that previous MRI scanning conditions...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2021· Randox Laboratories Ltd.

Recalled Item: RANDOX CHOL-cholesterol (total) test system intended to measure cholesterol...

The Issue: When calibrating using the standard provided in the kit, the change in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2021· Diversatek Healthcare

Recalled Item: Diversatek Health Recalled by Diversatek Healthcare Due to M-Catch Retrieval...

The Issue: M-Catch Retrieval Nets, Part Number 1175-01 / Lot Number 001919, that were...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2021· Philips North America Llc

Recalled Item: Wireless Footswtich used with the following Philips Allura Xper and Recalled...

The Issue: Wireless foot switch connection issues causing interruption of Fluoroscopy...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2021· NuVasive Specialized Orthopedics, Inc.

Recalled Item: NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System:...

The Issue: The Instructions for Use have been updated to include: (1) Clarification...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2021· Palodex Group Oy

Recalled Item: Orthopantomograph OP300 dental computed tomography x-ray system. The X-ray...

The Issue: It was noticed in production on 28.10.2021, that the final testing database...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2021· Osteomed, LLC

Recalled Item: OsteoMed OsteoPower Power Console: -OsteoMed OsteoPower Power Console 2 by...

The Issue: Due to consoles not in compliance with the latest electrical safety...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2021· Medline Industries Inc

Recalled Item: EVLP Convenience Pack/Kit Recalled by Medline Industries Inc Due to NaCl 250...

The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2021· Medline Industries Inc

Recalled Item: Venous Access Pack-LF Convenience Kit Recalled by Medline Industries Inc Due...

The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing