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. 2,496 recalls have been distributed to Connecticut in the last 12 months.
Showing 16381–16400 of 28,245 recalls
Recalled Item: PDS Plus Antibacterial (Polydioxanone) Suture Size 1 PDS PLUS Violet...
The Issue: Three (3) lots were distributed with the incorrect expiry date on the label....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PDS Plus Antibacterial (Polydioxanone) Suture Size 0 PDS Plus Violet...
The Issue: Three (3) lots were distributed with the incorrect expiry date on the label....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PDS Plus Antibacterial (Polydioxanone) Suture Size 0 PDS Plus Violet...
The Issue: Three (3) lots were distributed with the incorrect expiry date on the label....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RP RIVERPOINT MEDICAL 18G Brachy Grid B&K(TM) style Recalled by Riverpoint...
The Issue: Product is labeled with "CE", but is not yet approved in the European Union.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diagnostic Ultrasound System Recalled by Toshiba American Medical Systems...
The Issue: The power supply unit may be damaged and may fail to start up when the power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioMerieux mini VIDAS System in combination with Quality Control VIDAS*...
The Issue: Increase of events affecting performance regarding pump clogging and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper systems with Certeray X-ray Generator located in regions...
The Issue: There is an increase in the failure rate of certain Anode Drive Units (ADU5)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioMerieux VIDAS System in combination with Quality Control VIDAS* (QCV*)...
The Issue: Increase of events affecting performance regarding pump clogging and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance Big Bore Oncology CTwith 4.2.0 software version. Model #'...
The Issue: Software issues including: Software errors that may result in Extended Field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance Big Bore Radiology CT with 4.2.0 software version. Model Recalled...
The Issue: Software issues including: Software errors that may result in Extended Field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percuvance(R) Percutaneous Shaft 36cm Recalled by Teleflex Medical Due to...
The Issue: There is potential for a piece of the distal tip on the Percuvance shaft to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percuvance(R) Percutaneous Shaft 29cm Recalled by Teleflex Medical Due to...
The Issue: There is potential for a piece of the distal tip on the Percuvance shaft to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE ¿ /IMMULITE ¿ 1000 OM-MA (CA125) Recalled by Siemens Healthcare...
The Issue: Concentrations for the level of biotin that does not interfere is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE ¿ /IMMULITE ¿ 1000 TG Recalled by Siemens Healthcare Diagnostics,...
The Issue: Concentrations for the level of biotin that does not interfere is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE ¿ /IMMULITE ¿ 1000 BR-MA (CA15-3) Recalled by Siemens Healthcare...
The Issue: Concentrations for the level of biotin that does not interfere is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista¿ Mass Creatine Kinase (MMB) Flex¿ reagent cartridge Recalled...
The Issue: Concentrations for the level of biotin that does not interfere is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000/IMMULITE ¿ 2000 XPi OM-MA (CA125) Recalled by Siemens...
The Issue: Concentrations for the level of biotin that does not interfere is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur¿ Cyclosporine Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: The concentrations for biotin listed in the non-interfering substances...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista¿ Cardiac Troponin I (CTNI) Flex¿ reagent cartridge Recalled...
The Issue: Concentrations for the level of biotin that does not interfere is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE ¿ 2000/IMMULITE ¿ 2000 XPi Anti HBc Recalled by Siemens Healthcare...
The Issue: Concentrations for the level of biotin that does not interfere is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.