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 46381–46400 of 51,038 recalls
Recalled Item: Advanta SST Grafts <6mm Intended for use in arterial vascular reconstruction...
The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advanta SST Grafts >or= 6mm Intended for use in arterial Recalled by Atrium...
The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flixene IFG Vascular Grafts >or= 6mm Intended for use in Recalled by Atrium...
The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Vector TAS 8mm Screw. The Device Listing Number Recalled by...
The Issue: Ormco Corporation is voluntarily recalling one lot of 8 MM Vector TAS Screws...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OLA Buffer For Laboratory Use Recalled by Celera Corporation Due to The...
The Issue: The package insert for FG OLA Buffer, GPR displayed the wrong concentration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IsoGel AIR 84 Recalled by Stryker Medical Division of Stryker Corporation...
The Issue: Complaints were received from the field indicating that some Air Pumps were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AperFix AM Femoral Implant Recalled by Cayenne Medical Inc. Due to Potential...
The Issue: Potential for AperFix 24 mm implant breaking inside the drilled femoral socket.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...
The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...
The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...
The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...
The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...
The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acuson SC2000 volume imaging ultrasound systems at software version 3.0....
The Issue: Software issue results in inaccurate 3D image may result in ablation in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tempa DOT Single-Use Clinical Thermometer Medical Indicators Made in U.S.A....
The Issue: TempaDot products may have been mislabeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Microtainer Quikheel Lancet 1.0 mm incision Depth 2.5 mm Recalled by...
The Issue: The Lancet will not retract after activation thus creating a potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rultract Retractor Ratchet Cover Plate Distributed by Pemco Recalled by...
The Issue: The firm became aware of the problem when a ratchet cover plate on a device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liquid Yeast Cream Recalled by American Yeast Corporation Due to Potential...
The Issue: Bulk liquid yeast is contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Tray Surgical Recalled by Medtronic Xomed, Inc. Due to The firm will recall...
The Issue: The firm will recall and replace the identified instrument trays in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrepStain AG. For use in the screening and detection of cervical cancer....
The Issue: PrepStain system rack setting was incorrectly entered on one PrepStain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrepStain Tecan US-II. For use in the screening and detection Recalled by...
The Issue: PrepStain system rack setting was incorrectly entered on one PrepStain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.