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. 1,074 recalls have been distributed to Connecticut in the last 12 months.
Showing 14561–14580 of 51,038 recalls
Recalled Item: Premier Rotaclone Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: Product stored incorrectly in temperature controlled setting instead of .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Michels Transport Medium Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Product stored incorrectly in temperature controlled setting instead of .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neodent Easypack Helix GM Acqua 3.5X13/Smart 4.5X2.5 Article Number: 138.107...
The Issue: Mislabeled: Carton box item 138.089- Easypack Helix GM Acqua 3.5X8/Smart...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neodent Easypack Helix GM Acqua 3.5X8/Smart 4.5X2.5 -intended for dental...
The Issue: Mislabeled: Carton box item 138.089- Easypack Helix GM Acqua 3.5X8/Smart...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stanbio TDM/B-Hydroxybutyrate Tri-Level Controls Recalled by MEDLINE...
The Issue: Affected product was shipped from the warehouse at room temperature instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Box Label: activ5 TINY GYM IN YOUR POCKET activbody Model: Recalled by...
The Issue: Due to: 1) Manufacturing issue that result in inaccurate force measurement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regard Recalled by ROi CPS LLC Due to Kits lacks rubber latex warning label.
The Issue: Kits lacks rubber latex warning label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: activforce 2 package labeling: Model: Activ5-M R 201-200563 Recalled by...
The Issue: Due to: 1) Manufacturing issue that result in inaccurate force measurement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lidocaine Hydrochloride Recalled by Teligent Pharma, Inc. Due to Superpotent...
The Issue: Superpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine Hydrochloride Recalled by Teligent Pharma, Inc. Due to Superpotent...
The Issue: Superpotent Drug: Minimally superpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% Dextrose Injection Recalled by Pfizer Inc. Due to Lack of sterility...
The Issue: Lack of sterility assurance: bag has the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Moxifloxacin Recalled by Denver Solutions, LLC DBA Leiters Health Due to...
The Issue: Labeling: Label Mix-up: Vials labeled as moxifloxacin 1 mg/mL may actually...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diclofenac Sodium Topical Solution Recalled by Preferred Pharmaceuticals,...
The Issue: Defective container: Out of specification for container integrity leading to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cardinal Infant Heel Warmer Recalled by Philips North America Llc Due to...
The Issue: After the device was cleared by the FDA, Philips made changes to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heel Snuggler Recalled by Philips North America Llc Due to After the device...
The Issue: After the device was cleared by the FDA, Philips made changes to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medichoice Infant Heel Warmer Recalled by Philips North America Llc Due to...
The Issue: After the device was cleared by the FDA, Philips made changes to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infant Heel Warmers w/strap Recalled by Philips North America Llc Due to...
The Issue: After the device was cleared by the FDA, Philips made changes to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infa-Therm Transport Mattress Recalled by Philips North America Llc Due to...
The Issue: After the device was cleared by the FDA, Philips made changes to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triathlon Pro Tibial Preparation Tray Recalled by Howmedica Osteonics Corp....
The Issue: Triathlon Pro Tibial Preparation Tray may have been kitted with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura CV20 Interventional Fluoroscopic X-ray System products with a...
The Issue: Due to a leak in the detector cooling system, cooling liquid may leak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.