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. 2,623 recalls have been distributed to Connecticut in the last 12 months.
Showing 7661–7680 of 28,245 recalls
Recalled Item: Baxter CLEARLINK System Recalled by Baxter Healthcare Corporation Due to...
The Issue: Firm noted an increase in customer reports of leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Subdermal Needle Electrode Recalled by Technomed Europe Due to...
The Issue: Burns of varying degrees can occur to patients with electrodes left in while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CorVocet Biopsy System/Catalog Code: CORA1610/B Recalled by Merit Medical...
The Issue: Biopsy Systems have components that are misaligned due to an issue with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CorVocet Biopsy System Recalled by Merit Medical Systems, Inc. Due to Biopsy...
The Issue: Biopsy Systems have components that are misaligned due to an issue with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker EVOLVE Recalled by Wright Medical Technology, Inc. Due to The outer...
The Issue: The outer label does not match the device inside the package. The affected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker EVOLVE Recalled by Wright Medical Technology, Inc. Due to The outer...
The Issue: The outer label does not match the device inside the package. The affected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE CLEARPRO TRACH T-PIECE CLOSED SUCTION CATHETER Recalled by MEDLINE...
The Issue: Potential for the suction catheter to come apart from the green connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE CLEARPRO TRACH DOUBLE SWIVEL CLOSED SUCTION CATHETER Recalled by...
The Issue: Potential for the suction catheter to come apart from the green connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE CLEARPRO DOUBLE SWIVEL CLOSED SUCTION CATHETER Recalled by MEDLINE...
The Issue: Potential for the suction catheter to come apart from the green connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FABCO ORS DENTAL ROLLS Recalled by Carwild Corporation Due to Sterility with...
The Issue: Sterility with new cotton source not validated
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Randox Serology I Positive Control contains the following analytes...
The Issue: ***Update** :HBsAg analyte is also Non-Reactive on the Ortho Vitros analyser...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5 IN (17 cm) APPX 0.78 ml Recalled by ICU Medical, Inc. Due to Due to a...
The Issue: Due to a manufacturing defect which results in a visible gap between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroClave Clear Neutral Connector Recalled by ICU Medical, Inc. Due to Due...
The Issue: Due to a manufacturing defect which results in a visible gap between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6" (15 cm) Appx 0.85 ml Recalled by ICU Medical, Inc. Due to Due to a...
The Issue: Due to a manufacturing defect which results in a visible gap between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroClave Clear Neutral Connector. A bidirectional connector used as an...
The Issue: Due to a manufacturing defect which results in a visible gap between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8.5" (22 cm) Appx 0.85 ml Recalled by ICU Medical, Inc. Due to Due to a...
The Issue: Due to a manufacturing defect which results in a visible gap between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5" (17 cm) Appx 0.84 ml Recalled by ICU Medical, Inc. Due to Due to a...
The Issue: Due to a manufacturing defect which results in a visible gap between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The product is a handheld ultraviolet-C germicidal wand and contains two...
The Issue: Excessive ultraviolet-C radiation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number: 6028...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freeman Pancreatic Flexi-Stent Kits: Single Pigtail Catalog Number: 6501...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.