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. 2,092 recalls have been distributed to Connecticut in the last 12 months.
Showing 2381–2400 of 28,245 recalls
Recalled Item: Brand Name: VITROS Product Name: VITROS 5600 Integrated System Model/Catalog...
The Issue: The VITROS 5600 Integrated System software versions 3.8.0 may not correctly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: VITROS Product Name: VITROS XT 7600 Integrated System Recalled...
The Issue: The VITROS XT 7600 Integrated System software versions 3.8.0 may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: VITROS Product Name: VITROS 3600 Immunodiagnostic System...
The Issue: The VITROS 3600 Immunodiagnostic System software versions 3.8.0 may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PCR Cartridges used with MAX System. Model Number: 437519 Recalled by...
The Issue: Potential for signal drift in specific lots of BD PCR Cartridges.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz - Endoskope - - Optical Biopsy and Grasping Forceps Recalled by...
The Issue: Due to failure of manual cleaning validation, biopsy and grasping forceps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Due to an increase in...
The Issue: Due to an increase in complaints for pitch cable failures related to forceps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Due to an increase in...
The Issue: Due to an increase in complaints for pitch cable failures related to forceps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Miltex Cryosolutions Cartridges 4 Pack (23.5g N2O each) Recalled by...
The Issue: During the assembly of the cartridge to its connecting body part, the valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Miltex CryoSolutions Cartridges 10 Pack (23.5g N2O each) Recalled by...
The Issue: During the assembly of the cartridge to its connecting body part, the valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.