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. 960 recalls have been distributed to Rhode Island in the last 12 months.
Showing 31501–31520 of 47,970 recalls
Recalled Item: Syngo.x picture archiving and communication system Syngo.x is a software...
The Issue: Software error. Incorrect values for the volume calculation from a freehand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nylon Surgical Suture for human use and vet use Recalled by Riverpoint...
The Issue: Nylon Surgical Sutures are recalled because the seals may become open during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareLink iPro Version 1.10 Recalled by Medtronic Inc. Due to Medtronic...
The Issue: Medtronic MiniMed is recalling the CareLink iPro Therapy Management Software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Claravis (isotretinoin capsules USP) Recalled by Teva North America Due to...
The Issue: Failed Impurities/Degradation Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bupivacaine Hydrochloride Inj. Recalled by Hospira Inc., A Pfizer Company...
The Issue: Presence of particulate matter: Confirmed customer report for the presence...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: buPROPion Hydrochloride Extended-Release Tablets Recalled by Amerisource...
The Issue: Failed dissolution specifications - the out of specification result for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mozobil (plerixafor injection) 24 mg/1.2 mL (20 mg/mL) per vial Recalled by...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MISAGO RX Self Expanding Peripheral Stem Recalled by Terumo Medical Corp Due...
The Issue: During recent routine testing, the MISAGO Peripheral Stent was found not to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System Recalled by...
The Issue: Beckman Coulter is recalling the UniCel DxH Slidemaker Stainer Coulter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD¿ Piston Syringe Recalled by C.R. Bard, Inc. Due to Package Defect:...
The Issue: Package Defect: Products may be at risk for having a slit defect on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD¿ 70cc Piston Syringe with Catheter Tip Recalled by C.R. Bard, Inc. Due...
The Issue: Package Defect: Products may be at risk for having a slit defect on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD¿ Irrigation Recalled by C.R. Bard, Inc. Due to Package Defect: Products...
The Issue: Package Defect: Products may be at risk for having a slit defect on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARDIA¿ 60cc Piston Irrigation Syringe Recalled by C.R. Bard, Inc. Due to...
The Issue: Package Defect: Products may be at risk for having a slit defect on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista¿ Calcium (CA) Flex¿ reagent cartridge Device Listing No.:...
The Issue: Siemens Healthcare Diagnostics determined that the Dimension Vista Calcium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5 mm HYDRO LeMaitre Valvulotome Recalled by LeMaitre Vascular, Inc. Due to...
The Issue: Wire which deploys the loop may be come detached at the handle causing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5 mm HYDRO LeMaitre Valvulotome without LeMills Recalled by LeMaitre...
The Issue: Wire which deploys the loop may be come detached at the handle causing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5 mm HYDRO LeMaitre Valvulotome Recalled by LeMaitre Vascular, Inc. Due to...
The Issue: Wire which deploys the loop may be come detached at the handle causing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grassfields Country Dill Cheese Recalled by Whole Foods Market Due to...
The Issue: Possible contamination with Shiga toxin-producing E. coli (STEC).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Grassfields Leyden Cheese Recalled by Whole Foods Market Due to Potential E....
The Issue: Possible contamination with Shiga toxin-producing E. coli (STEC).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Grassfields Gouda Cheese Recalled by Whole Foods Market Due to Potential E....
The Issue: Possible contamination with Shiga toxin-producing E. coli (STEC).
Recommended Action: Do not consume. Return to store for a refund or discard.