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. 2,636 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,636 in last 12 months

Showing 60016020 of 28,245 recalls

Medical DeviceMay 31, 2023· Remel, Inc

Recalled Item: Remel Haemophilus Test Medium (Agar) (150mm) Recalled by Remel, Inc Due to...

The Issue: The test medium may not perform as intended.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2023· Synovo Production

Recalled Item: Femoral Resurfacing Cup - (xx)MM Recalled by Synovo Production Due to...

The Issue: Medical device components were marketed without FDA clearance

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2023· Synovo Production

Recalled Item: ACETABULAR FIXATION CUP Recalled by Synovo Production Due to Medical device...

The Issue: Medical device components were marketed without FDA clearance and without...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2023· Synovo Production

Recalled Item: ACETABULAR BEARING (xx)MM I.D X (xx) O.D. UHMWPE 1020 Recalled by Synovo...

The Issue: Medical device components were marketed without FDA clearance

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2023· Abbott Laboratories

Recalled Item: Alinity ci-series System Control Module Recalled by Abbott Laboratories Due...

The Issue: There are potential performance issues found in the Alinity ci-series System...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2023· Johnson & Johnson Surgical Vision, Inc.

Recalled Item: VERITAS Advanced Infusion Packs (VRT-AI) and VERITAS Advanced Fluidics Packs...

The Issue: Weld protrusion/physical gap between the housing and pack cover, may exceed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2023· DeRoyal Industries Inc

Recalled Item: Custom medical procedure packs labeled as: a) STURDI STRAINER TRAY STANDARD...

The Issue: The outer package seal could be open, or compromised which affects the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2023· DeRoyal Industries Inc

Recalled Item: Custom medical procedure packs labeled as: a) CATH ANGIOGRAPHY DRAPE PACK...

The Issue: The outer package seal could be open, or compromised which affects the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2023· DeRoyal Industries Inc

Recalled Item: Custom medical procedure packs labeled as: a) OPEN HEART TRACECART Recalled...

The Issue: The outer package seal could be open, or compromised which affects the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2023· DeRoyal Industries Inc

Recalled Item: Custom medical procedure packs labeled as: a) PELVIC EXAM TRAY Recalled by...

The Issue: The outer package seal could be open, or compromised which affects the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2023· DeRoyal Industries Inc

Recalled Item: Custom medical procedure packs labeled as: a) STANDARD OB PACK ASCENSION WI...

The Issue: The outer package seal could be open, or compromised which affects the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2023· Limacorporate S.p.A

Recalled Item: .14.800 Recalled by Limacorporate S.p.A Due to Due to manufacturing issue,...

The Issue: Due to manufacturing issue, their is a potential for peripheral holes to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2023· Limacorporate S.p.A

Recalled Item: .14.500 Recalled by Limacorporate S.p.A Due to Due to manufacturing issue,...

The Issue: Due to manufacturing issue, their is a potential for peripheral holes to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus Endoscope Reprocessor OER-Mini-For use in cleaning and high-level...

The Issue: Revised OER-Pro, OER-Elite, OER-Mini endoscope reprocessor labeling- the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2023· Olympus Corporation of the Americas

Recalled Item: Tracheal Intubation Fiberscope OLYMPUS LF-P- To be used with an Recalled by...

The Issue: Revised OER-Pro, OER-Elite, OER-Mini endoscope reprocessor labeling- the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus Endoscope Reprocessor OER-Elite-For use in cleaning and high-level...

The Issue: Revised OER-Pro, OER-Elite, OER-Mini endoscope reprocessor labeling- the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2023· Olympus Corporation of the Americas

Recalled Item: VISERA Tracheal Intubation Videoscope OLYMPUS LF Type V- For airway Recalled...

The Issue: Revised OER-Pro, OER-Elite, OER-Mini endoscope reprocessor labeling- the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus Endoscope Reprocessor OER-Pro-For use in cleaning and high-level...

The Issue: Revised OER-Pro, OER-Elite, OER-Mini endoscope reprocessor labeling- the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2023· Abiomed, Inc.

Recalled Item: Abiomed 14Fr Low Profile Introducer Set Recalled by Abiomed, Inc. Due to...

The Issue: There was one complaint that the sidearm of the device detached during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2023· Boston Scientific Corporation

Recalled Item: Flexiva Pulse 242 TracTip Single-Use Laser Fibers -intended to be Recalled...

The Issue: Manufactured with the incorrect component may result in lower power output...

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

Class II — Potential Health HazardOngoing