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.

51,038 total recalls
2,485 in last 12 months

Showing 1828118300 of 28,245 recalls

Medical DeviceMarch 3, 2017· Covidien LLC

Recalled Item: Covidien Curity Eye Pad Item Code: 03201 The sterile eye Recalled by...

The Issue: Product sterility is compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Covidien LLC

Recalled Item: Covidien Curity Saline Dressing 8' x 4 (20.3cm x10.2 cm) Recalled by...

The Issue: Product sterility is compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Integra LifeSciences Corp.

Recalled Item: Panta Nail Recalled by Integra LifeSciences Corp. Due to Voluntary...

The Issue: Voluntary recall/Removal of Panta and Panta XI Nails because there may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Cardiovascular Systems Inc

Recalled Item: ViperWire Advance Peripheral Guide Wire with Flex Tip Recalled by...

The Issue: Cardiovascular Systems, Inc. is recalling one lot of ViperWire Advance with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Implant Direct Sybron Manufacturing, LLC

Recalled Item: ImplantDirect Recalled by Implant Direct Sybron Manufacturing, LLC Due to...

The Issue: The main vial label lists the incorrect part number, but the cap label is...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Bausch & Lomb Inc Irb

Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...

The Issue: The complaints database was reviewed and there have been an atypical volume...

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

Class II — Potential Health HazardOngoing