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 25481–25500 of 27,456 recalls
Recalled Item: A) Product Code 2N1191: Non-DEHP Y-Type Catheter Extension Set Recalled by...
The Issue: Customers have reported that when separating an individual package from its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioMend¿ Extend" Absorbable Collagen Membrane BioMend¿ Extend" Absorbable...
The Issue: Due to the process deviation, product lots in question may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wallace Sure-Pro/ Sure-Pro Ultra Embryo Replacement Catheters (with...
The Issue: Unable to pass catheter through outer sheath during embryo transfer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeliTape Absorbable Collagen Wound Dressing for Dental Surgery The...
The Issue: Due to the process deviation, product lots in question may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integrity 1.1. Integrity is the interface and control software for Recalled...
The Issue: The problem is that the "static tolerances" from the calibration files...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeliPlug Absorbable Collagen Wound Dressing for Dental Surgery The...
The Issue: Due to the process deviation, product lots in question may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Spine ISSYS LP Inverted Screw System. 8.5MM X 45 Recalled by Custom...
The Issue: On March 28, 2013, Custom Spine, Inc. issued a minor removal of a lot of 18...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A) Product Code 2N8220: Non-DEHP Catheter Extension Set Kit Recalled by...
The Issue: Customers have reported that when separating an individual package from its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The CEP 8 SpectrumGreen (SG) ASR Probe Kit Recalled by Abbott Molecular Due...
The Issue: 20 kits of CEP 8 SG ASR Probe (list 06J37-018, lot 440023), contained Vysis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wallace Sure-Pro¿ Two Stage Embryo Replacement Catheter for difficult...
The Issue: Unable to pass catheter through outer sheath during embryo transfer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A) Product Code 2N3371: Non-DEHP Y-Type Catheter Extension Set Recalled by...
The Issue: Customers have reported that when separating an individual package from its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helistat Absorbable Hemostatic Recalled by Integra LifeSciences Corporation...
The Issue: Due to the process deviation, product lots in question may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HCS3011 AV Loop Kit For use with Transonic CO status System Only Recalled by...
The Issue: Transonic Systems Inc. have received complaints of blood leakage involving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Howmedica Osteonics Corp. AxSOS System Instrument. The AxSOS Locking...
The Issue: Stryker Orthopaedics has received a report indicating that the scale of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wallace Sure-Pro Ultra¿ Embryo Replacement Catheter with Stylet Product...
The Issue: Unable to pass catheter through outer sheath during embryo transfer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Suturable DuraGen Dural Regenerative Matrix Suturable DuraGen Dural...
The Issue: Due to the process deviation, product lots in question may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INSTAT - Agent Recalled by Integra LifeSciences Corporation Due to Due to...
The Issue: Due to the process deviation, product lots in question may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DuraGen Plus Dural Regeneration Matrix DuraGen Plus Adhesion Barrier Matrix...
The Issue: Due to the process deviation, product lots in question may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colla Tape Absorbable Collagen Wound Dressing for Dental Surgery The...
The Issue: Due to the process deviation, product lots in question may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wallace Sure-Pro¿ Two Stage Embryo Replacement Catheter with Obturator...
The Issue: Unable to pass catheter through outer sheath during embryo transfer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.