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. 2,472 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,472 in last 12 months

Showing 1972119740 of 28,245 recalls

Medical DeviceJune 23, 2016· The Metrix Company

Recalled Item: Container fill and transfer sets Recalled by The Metrix Company Due to An...

The Issue: An issue was identified after a redesign of the auto compounding device. The...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· The Metrix Company

Recalled Item: Dual Chamber Container fill with gravity/attached transfer sets Recalled by...

The Issue: An issue was identified after a redesign of the auto compounding device. The...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2016· The Metrix Company

Recalled Item: Container fill and transfer sets Recalled by The Metrix Company Due to An...

The Issue: An issue was identified after a redesign of the auto compounding device. The...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2016· LeMaitre Vascular, Inc.

Recalled Item: Anasto AC Closure System and Anasto Universal Clip Remover- Anasto Recalled...

The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2016· Draeger Medical, Inc.

Recalled Item: Babytherm 8004/8010 Recalled by Draeger Medical, Inc. Due to Risk associated...

The Issue: Risk associated with operating the device in skin temperature mode with...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2016· LeMaitre Vascular, Inc.

Recalled Item: AnastoClip AC 8cm 35 Clips (1 Each} Large REF # Recalled by LeMaitre...

The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS Immunodiagnostic Products HBsAg Controls Recalled by Ortho-Clinical...

The Issue: The signal/cutoff (s/c) results may increase throughout the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceJune 22, 2016· LeMaitre Vascular, Inc.

Recalled Item: Anastoclip AC 8cm 35 Clips (1 Each} Medium REF # Recalled by LeMaitre...

The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2016· LeMaitre Vascular, Inc.

Recalled Item: AnastoCiip Universal Clip Remover (6 Pack} REF# e4001-00 The Anastoclip...

The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2016· Sorin Group USA, Inc.

Recalled Item: AORTIC ARCH CANNULA Recalled by Sorin Group USA, Inc. Due to Sorin Group USA...

The Issue: Sorin Group USA is recalling Aortic Arch Cannulae (part numbers NA-55X7 and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2016· LeMaitre Vascular, Inc.

Recalled Item: AnastoCiip Universal Clip Remover (1Each} REF# e4001-04 The Anastoclip Clip...

The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2016· LeMaitre Vascular, Inc.

Recalled Item: AnastoCiip Universal Clip Remover (1Each} REF# 4001-04 The Anastoclip Clip...

The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2016· Olympus Scientific Solutions Americas

Recalled Item: Olympus Scientific Solutions Americas Corporation (OSSA) Model: Analytical...

The Issue: Trigger lock option does not always prevent x-ray generation. Specifically...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2016· LeMaitre Vascular, Inc.

Recalled Item: AnastoCiip Universal Clip Remover (6 Pack} REF# 4001-00 The Anastoclip...

The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2016· Stanley Security Solutions Inc

Recalled Item: Arial Wireless Water-Resistant Call Pendant The Arial Pendant tag is...

The Issue: Devices were incorrectly programmed during manufacturing therefore...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2016· MicroPort Orthopedics Inc.

Recalled Item: Conserve Cups: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...

The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceJune 21, 2016· MicroPort Orthopedics Inc.

Recalled Item: Lineage Shell: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...

The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceJune 21, 2016· Invacare Corporation

Recalled Item: lnvacare Precise Rx Pediatric Flowmeter Model Number: IRCPF16. Packed one...

The Issue: The rear gradation scale was screen printed upside down on the flowmeter gauge.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2016· MicroPort Orthopedics Inc.

Recalled Item: Lineage Liners: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...

The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceJune 21, 2016· MicroPort Orthopedics Inc.

Recalled Item: Cobalt Chromium Heads Transcend: 26000017 Recalled by MicroPort Orthopedics...

The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing