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. 1,875 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
1,875 in last 12 months

Showing 2822128240 of 51,038 recalls

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: rHead Recon Stem Implant non-coated 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 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: radial head implant #4 (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: 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: Radio Capitellum Small Recalled by Howmedica Osteonics Corp. Due to Revision...

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· Medacta Usa Inc

Recalled Item: The GMK knee system: designed for cemented use in total Recalled by Medacta...

The Issue: Medacta has observed a worldwide occurrence rate of post-operative insert...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Radiometer America Inc

Recalled Item: ABL800 analyzer with FLEXQ module. Device intended for in vitro Recalled by...

The Issue: Due to misinterpretation of the barcode by the scanner, when the...

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 Recalled by Howmedica Osteonics Corp. Due to Revision rate identified...

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· Smith & Nephew, Inc.

Recalled Item: smith&nephew TRIGEN INTERTAN 10S Recalled by Smith & Nephew, Inc. Due to A...

The Issue: A single lot of INTERTAN 10S 10 MM X 18 CM 130 D was manufactured with the...

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 Standard Extended Stem 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: rHead Recalled by Howmedica Osteonics Corp. Due to Revision rate identified...

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: 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 Recon Extended Stem Size 2. 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· Zimmer Biomet, Inc.

Recalled Item: Persona Partial Knee Spacer Blocks To assist in partial knee Recalled by...

The Issue: Zimmer Biomet is conducting a medical device recall for the Persona Partial...

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: 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