Product Recalls in Connecticut
Product recalls affecting Connecticut — including food, drugs, consumer products, medical devices, and vehicles distributed to Connecticut. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,054 recalls have been distributed to Connecticut in the last 12 months.
Showing 16701–16720 of 51,038 recalls
Recalled Item: InterV 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: 11G 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: InterV 10G Bone Access Tools/Kit Recalled by Zavation Due to Products...
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 Bipedicular Bone Access Kit with Drill 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: 10 G Coxaxial Cannula with Tuohy Connection 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: 10G BEVELED TROCAR/CANNULA. For use in Orthopedic / spinal procedures....
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: CEMIX - CEMENT MIXING SYSTEM STERILE Recalled by Zavation Due to Products...
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 Cement Delivery Cannula Recalled by Zavation Due to Products...
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 Biopsy Device Recalled by Zavation Due to Products distributed as...
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: 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: 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: 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: 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: 8G DIRECT WORKING CANNULA BEVEL TIP Recalled by BIOPSYBELL S.R.L. Due to...
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: Spectrum Medical Quantum Standard heat exchanger Recalled by QURA S.R.L. Due...
The Issue: Product labeled as sterile may not have been adequately sterilized. In...
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.
Recalled Item: Cardiosave Hybrid IABP - Product Usage: used to inflate and Recalled by...
The Issue: There are cybersecurity vulnerabilities in a widely used low-level TCP/IP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.