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. 2,445 recalls have been distributed to Connecticut in the last 12 months.
Showing 26281–26300 of 51,038 recalls
Recalled Item: MAYFIELD Infinity XR2 Base Unit-Extended Recalled by Integra LifeSciences...
The Issue: There is a potential for the knob assembly in the swivel adapter to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baby Quasar Plus Recalled by Quasar Bio-Tech, Inc. Due to Quasar did not...
The Issue: Quasar did not receive FDA clearance for claims of collagen/elastin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quasar MD Plus Recalled by Quasar Bio-Tech, Inc. Due to Quasar did not...
The Issue: Quasar did not receive FDA clearance for claims of collagen/elastin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pure Rayz Recalled by Quasar Bio-Tech, Inc. Due to Quasar did not receive...
The Issue: Quasar did not receive FDA clearance for claims of collagen/elastin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAYFIELD INFINITY XR2 BASE UNIT Recalled by Integra LifeSciences Corp. Due...
The Issue: There is a potential for the knob assembly in the swivel adapter to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica Sample Handler Additional (SMN 11069004). The Atellica" Solution is...
The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminex Aries M1 System Model: Aries M6V1 Aries Software v1.0 Recalled by...
The Issue: An incorrect control board and firmware installed in some of the Hand Held...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sisel Recalled by Sisel International Llc Due to Firm is recalling SiselRipt...
The Issue: Firm is recalling SiselRipt due to the presence of an unapproved artificial...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Prescript-Assist Broad Spectrum Probiotic & Prebiotic Gastrointestinal...
The Issue: The recalled dietary supplement has the potential to contain undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wish Bone House Italian Salad Dressing 15 oz. Recalled by Pinnacle Food...
The Issue: The recall was initiated after learning from a retail customer that a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The Neonatal Flow Sensor Cable used on devices CARESCAPE R860 Recalled by...
The Issue: The Neonatal Flow Sensor Cable may be missing the connector housing exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Daptomycin for Injection Recalled by PFIZER Due to Microbial Contamination...
The Issue: Microbial Contamination of Sterile Products: Product associated with reports...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nitrofurantoin Oral Suspension USP Recalled by LUPIN SOMERSET Due to...
The Issue: Subpotent Drug and Failed Content Uniformity.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Enalapril Maleate Recalled by Aidarex Pharmaceuticals LLC Due to...
The Issue: Out-of-specification results for the Enalapril Diketopiperazine degradation...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Enalapril Maleate Recalled by Aidarex Pharmaceuticals LLC Due to...
The Issue: Out-of-specification results for the Enalapril Diketopiperazine degradation...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Enalapril Maleate Recalled by Aidarex Pharmaceuticals LLC Due to...
The Issue: Out-of-specification results for the Enalapril Diketopiperazine degradation...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DigitalDiagnost 4 Flex / Value (Stitching Patient Support) 712028 Recalled...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus 235 Recalled by Ion Beam Applications S.A. Due to Gantry rotation or...
The Issue: Gantry rotation or proton irradiation can be allowed even if apertures or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BACT/ALERT VIRTUO system Recalled by bioMerieux, Inc. Due to The BACT/ALERT...
The Issue: The BACT/ALERT VIRTUO Instrument Firmware version R2.0 allows relocation of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BACT/ALERT VIRTUO system Recalled by bioMerieux, Inc. Due to The BACT/ALERT...
The Issue: The BACT/ALERT VIRTUO Instrument Firmware version R2.0 allows relocation of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.