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. 2,636 recalls have been distributed to Connecticut in the last 12 months.
Showing 5381–5400 of 28,245 recalls
Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...
The Issue: A backwards leak present in the integrated manometer of the patient valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD gravity sets (Product Name Recalled by Becton Dickinson & Company Due to...
The Issue: Affected infusion sets labeled as free of DEHP actually do contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...
The Issue: A backwards leak present in the integrated manometer of the patient valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Extension Sets (Product Name Recalled by Becton Dickinson & Company Due...
The Issue: Affected infusion sets labeled as free of DEHP actually do contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...
The Issue: A backwards leak present in the integrated manometer of the patient valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curaplex manual resuscitators with integrated manometer Recalled by SunMed...
The Issue: A backwards leak present in the integrated manometer of the patient valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VariSoft infusion set Recalled by Unomedical A/S Due to The Varisoft...
The Issue: The Varisoft infusion set is used in conjunction with tandem insulin pumps....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris Pump infusion sets (Product Name Recalled by Becton Dickinson &...
The Issue: Affected infusion sets labeled as free of DEHP actually do contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VariSoft infusion set Recalled by Unomedical A/S Due to The Varisoft...
The Issue: The Varisoft infusion set is used in conjunction with tandem insulin pumps....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...
The Issue: A backwards leak present in the integrated manometer of the patient valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NautilusTM ECMO Oxygenator with Balance Biosurface-used in extracorporeal...
The Issue: May have increased water path restriction within the heat exchanger, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NautilusTM Smart ECMO Module with Balance Biosurface-used in extracorporeal...
The Issue: May have increased water path restriction within the heat exchanger, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Product Code 6802413 and Product Recalled by...
The Issue: During planned monitoring of data post-release of Software Version 3.8.0 an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARDIOHELP Emergency Drive Recalled by Maquet Medical Systems USA Due to...
The Issue: Product removal due to possible blocking or impairment of the CARDIOHELP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 3600 Immunodiagnostic System Product Code 6802783 and Product...
The Issue: During planned monitoring of data post-release of Software Version 3.8.0 an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 7600 Integrated System Product Code 6844461 Running Software...
The Issue: During planned monitoring of data post-release of Software Version 3.8.0 an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stay Safe Cap Recalled by Fresenius Medical Care Holdings, Inc. Due to...
The Issue: Updating the labeling to include additional warnings and contraindications...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System Product Code 6802445 and Product Recalled by...
The Issue: During planned monitoring of data post-release of Software Version 3.8.0 an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 3400 Chemistry System Product Code 6844458 Running Software...
The Issue: During planned monitoring of data post-release of Software Version 3.8.0 an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips EPIQ Diagnostic Ultrasound System Models: EPIQ 7G(model # 795200)...
The Issue: Their is the potential that diagnostic ultrasound systems operating with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.