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. 2,496 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,496 in last 12 months

Showing 1674116760 of 28,245 recalls

Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: rHead Recon Stem Implant 6mm Collar Recalled by Howmedica Osteonics Corp....

The Issue: Revision rate identified as higher than other proximal radial head...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: rHead Stem Implant 6mm Collar Recalled by Howmedica Osteonics Corp. Due to...

The Issue: Revision rate identified as higher than other proximal radial head...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: radial stem implant #2 (Sterile packed). Orthopedic implant for replacement...

The Issue: Revision rate identified as higher than other proximal radial head...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: Lat Assembly Recalled by Howmedica Osteonics Corp. Due to Revision rate...

The Issue: Revision rate identified as higher than other proximal radial head...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: rHead Stem Implant Plasma Coated Recalled by Howmedica Osteonics Corp. Due...

The Issue: Revision rate identified as higher than other proximal radial head...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: Lateral Assembly Recalled by Howmedica Osteonics Corp. Due to Revision rate...

The Issue: Revision rate identified as higher than other proximal radial head...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: Lateral Assembly Recalled by Howmedica Osteonics Corp. Due to Revision rate...

The Issue: Revision rate identified as higher than other proximal radial head...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: Lateral Assembly Recalled by Howmedica Osteonics Corp. Due to Revision rate...

The Issue: Revision rate identified as higher than other proximal radial head...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: Radio Capitellum Broach Large Recalled by Howmedica Osteonics Corp. Due to...

The Issue: Revision rate identified as higher than other proximal radial head...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: Radio Capitellum Recalled by Howmedica Osteonics Corp. Due to Revision rate...

The Issue: Revision rate identified as higher than other proximal radial head...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: radial stem implant #2 (Sterile packed). Orthopedic implant for replacement...

The Issue: Revision rate identified as higher than other proximal radial head...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: #4 Bipolar stem implant (Sterile packed). Orthopedic implant for replacement...

The Issue: Revision rate identified as higher than other proximal radial head...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2017· Medline Industries Inc

Recalled Item: Sensicare Green Surgical Glove Recalled by Medline Industries Inc Due to...

The Issue: Possible open seal on top portion of the package. Could cause breach of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2017· Terumo BCT, Inc.

Recalled Item: HARVEST TERUMOBCT Recalled by Terumo BCT, Inc. Due to Certain lots of the...

The Issue: Certain lots of the Harvest Graft Delivery System GDP-10 Procedure Packs may...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Cook Inc.

Recalled Item: Mallinckrodt Institute Percutaneous Gastrostomy Set Product Usage: Intended...

The Issue: Cook has identified that the affected lots may contain wire guides that were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Cook Inc.

Recalled Item: Percutaneous Gastrojejunostomy Set Product Usage: Intended for the...

The Issue: Cook has identified that the affected lots may contain wire guides that were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Johnson & Johnson Vision Care, Inc.

Recalled Item: 1-DAY ACUVUE Moist for ASTIGMATISM Brand Contact Lenses Recalled by Johnson...

The Issue: Some contact lenses were associated with complaints of a foreign matter...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Johnson & Johnson Vision Care, Inc.

Recalled Item: ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR Recalled by Johnson &...

The Issue: Some contact lenses were associated with complaints of a foreign matter...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Cook Inc.

Recalled Item: Wills-Oglesby Percutaneous Gastrostomy Set Product Usage: Intended for the...

The Issue: Cook has identified that the affected lots may contain wire guides that were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Johnson & Johnson Vision Care, Inc.

Recalled Item: ACUVUE OASYS Brand Contact Lenses with HYDRACLEAR PLUS Recalled by Johnson &...

The Issue: Some contact lenses were associated with complaints of a foreign matter...

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

Class II — Potential Health HazardOngoing