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. 1,037 recalls have been distributed to Rhode Island in the last 12 months.
Showing 15461–15480 of 47,970 recalls
Recalled Item: ZVplasty System Recalled by Zavation Due to Products distributed as sterile...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZVplasty Directional Cement Cannula (4 pieces per pack) Recalled by Zavation...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZVplasty System Recalled by Zavation Due to Products distributed as sterile...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZVplasty Unipedicular Cement Delivery Cannula Kit Recalled by Zavation Due...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZVplasty System Recalled by Zavation Due to Products distributed as sterile...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10G DIRECT DOUBLE BONE ACCESS KIT. For use in Orthopedic / spinal...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10G SINGLE CEMENT DELIVERY KIT (5 FILLERS). For use in Recalled by Zavation...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZVPlasty Recalled by Zavation Due to Products distributed as sterile may not...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZVplasty Direct Access Diamond Tip Trocar Recalled by Zavation Due to...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10 GAUGE DIRECT UNILATERAL STYLET(1 X DIAMOND 1 X BEVEL) Recalled by...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZVplasty 10G Recalled by Zavation Due to Products distributed as sterile may...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZVplasty Recalled by Zavation Due to Products distributed as sterile may not...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PowerPort duo M.R.I. Implantable Port Recalled by Bard Peripheral Vascular...
The Issue: Catheters may experience difficulty in flushing, infusion, and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioGX SARS-CoV-2 Reagents for BD MAX System-IVD PCR test intended Recalled...
The Issue: BioGX SARS-CoV-2 Reagents for BD MAX" System rehydration buffer tubes were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aftermarket Alaris Infusion Pump Module Model 8100 Front Bezel Recalled by...
The Issue: Aftermarket front bezel components were installed during service/repair, not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drop Arm Versamode" Recalled by Gf Health Products Due to The front casters...
The Issue: The front casters on the 6810A Lumex Drop Arm Versamode are incorrect.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thumbs Up 7 Blue 69K Recalled by Bit & Bet LLC Due to Marketed without...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VenaSeal Closure System Recalled by Medtronic Inc. Due to Firm received...
The Issue: Firm received increased number of reports that VenaSeal dispensing systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CEMIX - CEMENT MIXING SYSTEM Recalled by BIOPSYBELL S.R.L. Due to Products...
The Issue: Products labeled as sterile were distributed, but may not have been sterilized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Normand Remisol Advance Data Manager is a software device that Recalled by...
The Issue: Instructions For Use for software versions 1.5 to 1.9 did not provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.