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. 2,356 recalls have been distributed to Connecticut in the last 12 months.
Showing 47481–47500 of 51,038 recalls
Recalled Item: Mini Cannulated Titanium Headed and Headless Screw Set and 2.5 Recalled by...
The Issue: Faded and wrong markings on bone screw Countersink/Depth Gauge instruments...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******iMRI Handpiece. Use with iMRI System Only***Rx Only***Manufacturer:...
The Issue: The firm Anspach Effort of Palm Beach Gardens, FL initiated a voluntary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******XMax Handpiece***Rx Only***Manufacturer: The Anspach Effort Recalled...
The Issue: The firm Anspach Effort of Palm Beach Gardens, FL initiated a voluntary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******Swivel/Angle Motor Assembly***Rx Only***The Anspach Effort Recalled by...
The Issue: The firm Anspach Effort of Palm Beach Gardens, FL initiated a voluntary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******microMax Handpiece***Rx Only***Manufacturer: The Anspach Effort...
The Issue: The firm Anspach Effort of Palm Beach Gardens, FL initiated a voluntary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension(R) TACR Flex(R) reagent cartridge (DF107) The TACR method is...
The Issue: Siemens has confirmed that the TACR method may demonstrate reduced on-board...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydra Vision DR 60/80 System Recalled by Leibel-Flarsheim Company LLC Due to...
The Issue: A complaint was received in which a hospital physicist indicated the dosage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B-CrossLaps/serum (B-CTx in serum) 160 100 tests Immunoassay Recalled by...
The Issue: Roche Diagnostics internal investigations in R&D have shown that the claims...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView SPECT gamma camera for Emission Computed Tomography Recalled by...
The Issue: Philips has received one report from the field that there was an unexpected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluoroscan Mini C-arm InSight Recalled by Hologic, Inc. Due to The audible...
The Issue: The audible alarm to alert the operator when cumulative irradiation time...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluoroscan Mini C-arm InSight2 Recalled by Hologic, Inc. Due to The audible...
The Issue: The audible alarm to alert the operator when cumulative irradiation time...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cornea Coat Recalled by Insight Instruments, Inc. Due to Marketed without an...
The Issue: Marketed without an Approved NDA/ANDA.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Early Bird Foods & Co. CHOC-A-DOODLE-DOO featuring DARK CHOCOLATE & Recalled...
The Issue: Early Bird Foods & Co. LLC is recalling CHOC-A-DOODLE-DOO featuring DARK...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: embla Embletta Gold (It functions as a Polysomnography Recorder and Recalled...
The Issue: Calibration error for Embla Embletta Gold units calibrated through service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXSTENT Femoropopliteal Self-Expanding Stent System. Product Usage: The...
The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXSTENT Biliary Self-Expanding Stent System. Product Usage: The FSS...
The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXSTENT Femoropopliteal Self-Expanding Stent System. Product Usage: The...
The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXSTENT Femoropopliteal Self-Expanding Stent System. Product Usage: The...
The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXSTENT Biliary Self-Expanding Stent System. Product Usage: The FSS...
The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glutathione 200mg/ml Inj SDV: 3x50ml 14 day expiration Recalled by Nora...
The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.