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 26121–26140 of 47,970 recalls
Recalled Item: Synvisc-One ¿ (hylan G-F 20) Recalled by Sanofi Genzyme Due to Contamination...
The Issue: Contamination with Methylbacterium thiocyanatum
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Guider Softip XF Guide Catheter Product Usage: Is Recalled...
The Issue: Potential polymer material degradation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Action Industries Inc. Blue OR Towel Non X-Ray Detectable Recalled...
The Issue: Product sterility potentially compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESCAPE R860 ventilators with software version 10SP05 Product Usage: The...
The Issue: Potential for the display processor to experience an unexpected failure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Shigella sonnei Phase 1 & 2 Agglutinating Serum Recalled by Remel Inc...
The Issue: The serum may fail to agglutinate within the specified minimum reaction time.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Humeral Stem 55mm(Size 13) Product Usage: Intended for primary and Recalled...
The Issue: Zimmer Biomet is conducting a medical device recall for two lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT c16000 Cuvette Segment Recalled by Abbott Laboratories, Inc Due to...
The Issue: There is a potential to generate falsely depressed patient results in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT c8000 Cuvette Segment Recalled by Abbott Laboratories, Inc Due to...
The Issue: There is a potential to generate falsely depressed patient results in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Humeral Stem 83mm(Size 17) Product Usage: Intended for primary and Recalled...
The Issue: Zimmer Biomet is conducting a medical device recall for two lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT c4000 Cuvette Segment Recalled by Abbott Laboratories, Inc Due to...
The Issue: There is a potential to generate falsely depressed patient results in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCOLADE EL DR Pacemaker Recalled by Boston Scientific Corporation Due to...
The Issue: Boston Scientific has received reports of intermittent over-sensing of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ESSENTIO MRI DR Pacemaker Recalled by Boston Scientific Corporation Due to...
The Issue: Boston Scientific has received reports of intermittent over-sensing of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCOLADE MRI DR Pacemaker Recalled by Boston Scientific Corporation Due to...
The Issue: Boston Scientific has received reports of intermittent over-sensing of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ESSENTIO EL DR Pacemaker Recalled by Boston Scientific Corporation Due to...
The Issue: Boston Scientific has received reports of intermittent over-sensing of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ALTRUA 2 EL DR Pacemaker Recalled by Boston Scientific Corporation Due to...
The Issue: Boston Scientific has received reports of intermittent over-sensing of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROPONENT VDD SL Pacemaker Recalled by Boston Scientific Corporation Due to...
The Issue: Boston Scientific has received reports of intermittent over-sensing of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ALTRUA 2 DR Pacemaker Recalled by Boston Scientific Corporation Due to...
The Issue: Boston Scientific has received reports of intermittent over-sensing of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROPONENT DR Pacemaker Recalled by Boston Scientific Corporation Due to...
The Issue: Boston Scientific has received reports of intermittent over-sensing of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VALITUDE X4 CRT-P Pacemaker Recalled by Boston Scientific Corporation Due to...
The Issue: Boston Scientific has received reports of intermittent over-sensing of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ESSENTIO MRI EL DR Pacemaker Recalled by Boston Scientific Corporation Due...
The Issue: Boston Scientific has received reports of intermittent over-sensing of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.