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 18801–18820 of 28,245 recalls
Recalled Item: Bariatric Bed - BARPKG-IVC 1633 Recalled by Invacare Corporation Due to A...
The Issue: A quality issue with the junction box used in the bariatric bed junction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Junction Box - 1104343 and 1193560 Recalled by Invacare Corporation Due to A...
The Issue: A quality issue with the junction box used in the bariatric bed junction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Special Connector Instruments (Special Connector Recalled by K2M, Inc...
The Issue: Instruments were developed without adequate consideration given to the need...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRU-Balance 3 Power Positioning Systems Recalled by Pride Mobility Products...
The Issue: The interface between the TB3 back and tilt base can separate when tilted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PreludeEASE Hydrophilic Sheath Introducer Dilator The Merit PreludeEASE...
The Issue: Recalling dilators included with the 6F PreludeEASE Hydrophilic Sheath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8470-009-030 3.0MM Precision Round Recalled by Stryker Instruments Div. of...
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8450-107-530 3.0MM Precision Match Head Recalled by Stryker Instruments Div....
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8450-010-040 4.0MM Round Recalled by Stryker Instruments Div. of Stryker...
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8450-009-030 3.0MM Precision Round Recalled by Stryker Instruments Div. of...
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8450-107-525 2.5MM Precision Match Head Recalled by Stryker Instruments Div....
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8450-009-040 4.0MM Precision Round Recalled by Stryker Instruments Div. of...
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8470-009-040 4.0MM Precision Round Recalled by Stryker Instruments Div. of...
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Medical Dual Chamber Ocean Drains as follows: 2020-000 Ocean Recalled...
The Issue: Outer Packaging is not sterile
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Medical Oasis Pediatric Drain as follows: 3612-100 Oasis...
The Issue: Outer Packaging is not sterile
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Medical Pediatric Chamber Ocean Drains as follows: 2012-320 Ocean...
The Issue: Outer Packaging is not sterile
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Medical 400 Series Express Drains as follows: 4000-100N Express...
The Issue: Outer Packaging is not sterile
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Medical Oasis Single Drain as follows: 3600-100 Oasis single Recalled...
The Issue: Outer Packaging is not sterile
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Medical 16400 Express Mini 500 dry seal drain Product Recalled by...
The Issue: Outer Packaging is not sterile
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Medical Ocean Blood Recovery Drains as follows: 2050-000 Ocean...
The Issue: Outer Packaging is not sterile
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes VA Implant Rack for the Compact Distal Radius System Recalled by...
The Issue: The screw rack plate was assembled incorrectly which could cause the screws...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.