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. 2,485 recalls have been distributed to Connecticut in the last 12 months.
Showing 17541–17560 of 28,245 recalls
Recalled Item: Accu2i pMTA Applicator Recalled by Angiodynamics, Inc. Due to The firm is...
The Issue: The firm is recalling product that has the potential to not function during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CER OPTION TYPE 1 TPR SLEVE -6 Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RED SEXP DSTL FEM 19CM RT ASSY Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lateral Troch Plate Full Crimp - 254mm Recalled by Zimmer Biomet, Inc. Due...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Humeral Guide Wire Ball Tip 2.4 mm Diameter 70 cm Length Recalled by Zimmer...
The Issue: The design verification for the previous packaging configuration G928 does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu2i pMTA Applicator Recalled by Angiodynamics, Inc. Due to The firm is...
The Issue: The firm is recalling product that has the potential to not function during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RED SEXP DSTL FEM 19CM LT ASSY Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim 5 Elite Recalled by St. Jude Medical, Inc. Due to The firm...
The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: St. Jude Medical. Agilis NxT Steerable Introducer: B1-Directional Recalled...
The Issue: Inadequate seal due to lack of adhesive glue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD DISPOZ-A-BAG Leg Bag with Flip-Flo Valve with Drain Extension Recalled...
The Issue: Customer complaint of a cut in the side of the leg bag, indicating a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity 5 Recalled by St. Jude Medical, Inc. Due to The firm discovered a...
The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity 7 Recalled by St. Jude Medical, Inc. Due to The firm discovered a...
The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity 5 Recalled by St. Jude Medical, Inc. Due to The firm discovered a...
The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity 7 Recalled by St. Jude Medical, Inc. Due to The firm discovered a...
The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim 7 Elite Recalled by St. Jude Medical, Inc. Due to The firm...
The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Xi Surgical System Product Usage: The da Vinci Recalled by...
The Issue: da Vinci Xi(R) Surgical System Patient Side Carts (PSC) were shipped to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW¿ PICC powered by ARROW¿ VPS¿ Stylet The Pressure Injectable Recalled...
The Issue: There is a possibility that the finished good kits may contain 5 Fr...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW¿ PICC powered by ARROW¿ VPS¿ Stylet The Pressure Injectable Recalled...
The Issue: There is a possibility that the finished good kits may contain 5 Fr...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ArrowADVANTAGE5" Pressure Injectable Peripherally Inserted Central Catheter...
The Issue: There is a possibility that the finished good kits may contain 5 Fr...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow(R) VPS(R) Access Kit for use with 4 Fr. Peripherally Recalled by Arrow...
The Issue: There is a possibility that the finished good kits may contain 5 Fr...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.