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. 2,447 recalls have been distributed to Rhode Island in the last 12 months.
Showing 16461–16480 of 27,456 recalls
Recalled Item: Mobile Mini C-arm system Part # 1000-0004. Intended to provide Recalled by...
The Issue: OrthoScan Inc. discovered during investigation of a non-standard work flow a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobile Mini C-arm system Part # 1000-0005. Intended to provide Recalled by...
The Issue: OrthoScan Inc. discovered during investigation of a non-standard work flow a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobile Mini C-arm system Part # 1000-0001. Intended to provide Recalled by...
The Issue: OrthoScan Inc. discovered during investigation of a non-standard work flow a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.via systems with SW VB20A Recalled by Siemens Medical Solutions USA,...
The Issue: A software update was released on August 22, 2017. Performing this software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carl Zeiss INTRABEAM PRS 500 Recalled by Carl Zeiss Meditec AG Due to The...
The Issue: The device had an incorrect printed calibration value on the calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer¿ K2 EDTA (K2E) 3.6mg Blood Collection Tube (13 Recalled by...
The Issue: A limited portion of the lot was manufactured with less than the required...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Partial Knee System Product Usage: The Persona Partial Knee Recalled...
The Issue: Potential for the Persona Partial Knee Impactor Pad to fracture.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fortify VR - Model Numbers: CD1231-40 and CD1231-40Q Recalled by St Jude...
The Issue: The device may exhibit premature battery depletion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unify Recalled by St Jude Medical Inc. Due to The device may exhibit...
The Issue: The device may exhibit premature battery depletion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGC 2000 LP Patella Recalled by Zimmer Biomet, Inc. Due to The affected AGC...
The Issue: The affected AGC 2000 LP Patella products were over-molded leaving the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGC 2000 LP Patella Recalled by Zimmer Biomet, Inc. Due to The affected AGC...
The Issue: The affected AGC 2000 LP Patella products were over-molded leaving the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G7 DUAL MOBILITY LINER 44MM F Product Usage: Intended for Recalled by Zimmer...
The Issue: The affected products are labeled and etched as F-44 mm liners; however, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AArtis Q/ Q.Zen biplane Artis zee biplane Product Usage: Artis Recalled by...
The Issue: Within a specific number of Artis zee biplane and Artis Q biplane systems, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lyophilized Chemistry Calibrator Level 1 Product Usage: Beckman Coulter...
The Issue: Unpaired lots of AU lyophilized chemistry calibrator level 1 and 2 have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Multi Measurement Server Recalled by Philips Electronics North...
The Issue: Distorted ST-Segment when using 12-Lead ECG Monitoring with Philips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.plaza systems with SW VB20A Recalled by Siemens Medical Solutions USA,...
The Issue: When a prior study is being replaced in the workflow step, in certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Recalled by Smiths Medical ASD Inc. Due to Potential for the...
The Issue: Potential for the syringe barrel clamp mechanism to loosen, decreasing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Recalled by Smiths Medical ASD Inc. Due to Potential for the...
The Issue: Potential for the syringe barrel clamp mechanism to loosen, decreasing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUIOS CL Flow Cytometer System The AQUIOS CL Flow Cytometer Recalled by...
The Issue: Beckman Coulter has identified that an incorrect setting using a proprietary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TCC-EZ Recalled by Integra LifeSciences Corp. Due to A quarantined lot of...
The Issue: A quarantined lot of the devices was released for sale. Devices from this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.