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 25041–25060 of 27,456 recalls
Recalled Item: pO2 D999 membrane units. Distributed by Radiometer America Recalled by...
The Issue: RADIOMETER became aware that the regarded lot pO2 units 942-042R0971 were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona (TM) The Personalized Knee System CR Tibial Articular Surface...
The Issue: Zimmer had received complaints that reported breakage of the Persona Knee...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: nanoFLEX CC4204A Intraocular Lens Correct aphakia in persons 60 years...
The Issue: STAAR Surgical Company is recalling a limited number of nanoFLEX CC4204A and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona (TM) The Personalized Knee System Tibial Articular Surface...
The Issue: Zimmer had received complaints that reported breakage of the Persona Knee...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge Assure Accufast BI Test Pack w/ 5 Controls Recalled by Steritec...
The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona (TM) The Personalized Knee System PS Tibial Articular Surface...
The Issue: Zimmer had received complaints that reported breakage of the Persona Knee...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal BI Stat Biological Test Pack with Instant Readout Integrator...
The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Osseotite 2 Certain Prevail 5mm(D)X 4.1mm (P) X X 11.5mm Recalled by Biomet...
The Issue: One of the dental implants do not have the internal hex feature. One of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Osseotite Parallel Walled Certain 4mm(D)X 15mm (L) Dental Implant Product...
The Issue: One of the dental implants do not have the internal hex feature. One of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona (TM) The Personalized Knee System Tibial Articular Surface...
The Issue: Zimmer had received complaints that reported breakage of the Persona Knee...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Steam Biological Indicators Recalled by Steritec Products Mfc. Co.,...
The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Steam Biological Indicator Recalled by Steritec Products Mfc. Co.,...
The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona (TM) The Personalized Knee System CPS Tibial Articular Surface...
The Issue: Zimmer had received complaints that reported breakage of the Persona Knee...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mesa Labs Smart-Read 10^5 EZ Test BI Test Pack Recalled by Steritec Products...
The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597106126 Provisional MIC POROUS PAT PROV 26MMX10MM Recalled by Zimmer,...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597201131 Femur CR POR SURF HDN FEM CO-NID AML Rx Recalled by Zimmer, Inc....
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00598706201 Provisional CRA FEM PROV/CUT GDE SZ BML Recalled by Zimmer, Inc....
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597102010 Provisional CR ART SURF PROV 12/PURPLE 10 Recalled by Zimmer,...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597502010 Provisional AC ART SURF PROV 12/PUR 10 Recalled by Zimmer, Inc....
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597602010 Articular Surface AC ART SURF 12/PUR 10 Recalled by Zimmer, Inc....
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.