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. 1,739 recalls have been distributed to Connecticut in the last 12 months.
Showing 48741–48760 of 51,038 recalls
Recalled Item: Berres Brothers Coffee Roasters Lunch with Elvis regular ground coffee...
The Issue: Berres Brothers Coffee Roasters is recalling 3 flavors of regular and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Berres Brothers Coffee Roasters Lunch with Elvis decaffeinated ground coffee...
The Issue: Berres Brothers Coffee Roasters is recalling 3 flavors of regular and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Berres Brothers Coffee Roasters Mocha Monkey regular ground coffee packaged...
The Issue: Berres Brothers Coffee Roasters is recalling 3 flavors of regular and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Berres Brothers Coffee Roasters Lunch with Elvis decaffeinated whole bean...
The Issue: Berres Brothers Coffee Roasters is recalling 3 flavors of regular and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Berres Brothers Coffee Roasters Mocha Monkey regular whole bean coffee...
The Issue: Berres Brothers Coffee Roasters is recalling 3 flavors of regular and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Berres Brothers Coffee Roasters Chocolate & Peanut Butter regular whole...
The Issue: Berres Brothers Coffee Roasters is recalling 3 flavors of regular and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Berres Brothers Coffee Roasters Chocolate & Peanut Butter Decaffeinated...
The Issue: Berres Brothers Coffee Roasters is recalling 3 flavors of regular and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The Vertex Max Drill Tube is a component within the Recalled by Medtronic...
The Issue: Medtronic is recalling certain Vertex Max Drill Tubes which are used with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica ASP6025 Vacuum Tissue Processor The Leica ASP6025 is a Recalled by...
The Issue: The Instruction for Use 1v9 and all previous versions specify incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Buffered Sodium Citrate (9NC) Plus Blood Collection Tubes...
The Issue: BD is conducting a recall of the BD Vacutainer 2.7mL Plus Citrate Blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Spine Ardis Inserter Recalled by Zimmer, Inc. Due to Zimmer Spine has...
The Issue: Zimmer Spine has received reports of the PEEK Ardis Interbody Spacer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biosense Webster MobiCath Bi-Directional Guiding Sheath. Small Curve catalog...
The Issue: Greatbatch Medical observed some anomalies of the inner lumen of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.