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. 2,496 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,496 in last 12 months

Showing 1126111280 of 47,970 recalls

Medical DeviceJuly 12, 2022· FUJIFILM Healthcare Americas Corporation

Recalled Item: Surpria 64: Software Version V3.11 Recalled by FUJIFILM Healthcare Americas...

The Issue: Error 00003050 or 00003052 may occur during scanning, the captured images...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2022· FUJIFILM Healthcare Americas Corporation

Recalled Item: SCENARIA View: Software Version V1.08 Recalled by FUJIFILM Healthcare...

The Issue: Error 00003050 or 00003052 may occur during scanning, the captured images...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2022· FUJIFILM Healthcare Americas Corporation

Recalled Item: Surpria: Software Version V3.11 Recalled by FUJIFILM Healthcare Americas...

The Issue: Error 00003050 or 00003052 may occur during scanning, the captured images...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Sensis or Sensis Vibe Combo systems as follows: System Recalled by...

The Issue: The Sensis Signal Input Box provides hooks as a milled item on the bottom of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 12, 2022· Haimen Shengbang Laboratory Equipment Co. Ltd.

Recalled Item: HXBL/WETEX/Genesis Biomedical Viral Transport Container Recalled by Haimen...

The Issue: Distributed VTM outside of VTM Guidance and without clearance.

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2022· Haimen Shengbang Laboratory Equipment Co. Ltd.

Recalled Item: HXBL/WETEX/Genesis Biomedical Viral Transport Container Recalled by Haimen...

The Issue: Distributed VTM outside of VTM Guidance and without clearance.

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2022· Haimen Shengbang Laboratory Equipment Co. Ltd.

Recalled Item: HXBL/WETEX/Genesis Biomedical Viral Transport Container Recalled by Haimen...

The Issue: Distributed VTM outside of VTM Guidance and without clearance.

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

Class I — Serious Health HazardOngoing
DrugJuly 11, 2022· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Tacrolimus Ointment Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: Defective Container: Tube split from side seam

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugJuly 11, 2022· Hikma Pharmaceuticals USA Inc.

Recalled Item: Ativan Injection (lorazepam injection Recalled by Hikma Pharmaceuticals USA...

The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2022· Hikma Pharmaceuticals USA Inc.

Recalled Item: Lorazepam Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2022· Hikma Pharmaceuticals USA Inc.

Recalled Item: Lorazepam Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2022· Hikma Pharmaceuticals USA Inc.

Recalled Item: Lorazepam Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 11, 2022· WISSNER-BOSSERHOFF GMBH

Recalled Item: SafeControl handset (a component of the Sentida bed which moves Recalled by...

The Issue: When the handset is disconnected from the power mains, and mains operation...

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

Class II — Potential Health HazardOngoing
DrugJuly 7, 2022· Apotex Corp.

Recalled Item: Aripiprazole Tablets Recalled by Apotex Corp. Due to Failed dissolution...

The Issue: Failed dissolution specifications: OOS for dissolution at the 12-month...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 7, 2022· Olympus Corporation of the Americas

Recalled Item: ShockPulse-SE Lithotripsy Generator Model/Serial: SPL-S Recalled by Olympus...

The Issue: Mis-wired component-the improperly wired component can result in additional...

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

Class II — Potential Health HazardOngoing
DrugJuly 5, 2022· Mylan Pharmaceuticals Inc

Recalled Item: Insulin Glargine (Insulin glargine-yfgn) Injection Recalled by Mylan...

The Issue: Labeling: Missing label: Label missing from some prefilled pens.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 5, 2022· TOVALA

Recalled Item: Tovala Gochujang-Glazed Pork Chop Bowl meal No.9-A Recalled by TOVALA Due to...

The Issue: Product contains undeclared peanut

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 5, 2022· TOVALA

Recalled Item: Tovala Gochujang-Glazed Salmon Bowl meal No.18-A Recalled by TOVALA Due to...

The Issue: Product contains undeclared peanut

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 5, 2022· Zap Surgical Systems

Recalled Item: ZAP-X Radiosurgery System Recalled by Zap Surgical Systems Due to Software...

The Issue: Software issue identified in cases of initial patient setup with large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2022· Medicina Uk Ltd

Recalled Item: Medicina Oral Tip Syringe 0.5ml Code: OT005 Recalled by Medicina Uk Ltd Due...

The Issue: Plunger component has been manufactured with an unapproved material...

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

Class II — Potential Health HazardOngoing