Product Recalls in District of Columbia

Product recalls affecting District of Columbia — including food, drugs, consumer products, medical devices, and vehicles distributed to District of Columbia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,448 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,448 in last 12 months

Showing 2568125700 of 27,451 recalls

Medical DeviceFebruary 25, 2013· Nova Biomedical Corporation

Recalled Item: Nova StatStrip Xpress Glu-Test Strips (Glucose test strips) Catalog #...

The Issue: Glucose test strips reports no result message when tested

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Lifescan Inc

Recalled Item: LifeScan brand OneTouch¿ Select Control Solution Recalled by Lifescan Inc...

The Issue: When OneTouch¿ Ultra and OneTouch¿ Select test strips are tested with Ultra...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2013· Clinical Diagnostic Solutions

Recalled Item: Boule Con-Diff Tri-Level Multi-Parameter Assayed Hematology Control Recalled...

The Issue: Elevated MCV results on the 1311-682, 1311-683, and 1311-684 lots.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2013· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Baseplate Impactor Extractor TRIATHLON Instruments....

The Issue: Stryker received reports from the field indicating that the handle detached...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes 11-Hole Recalled by Synthes USA HQ, Inc. Due to The Synthes...

The Issue: The Synthes One-Third Tubular DCL Plate (11-Hole, 1/3 Tubular Plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2013· Aperio Technologies Inc

Recalled Item: Aperio ScanScope System. Aperio ScanScope Models Recalled by Aperio...

The Issue: Aperio initiated this recall because the User Guides incorrectly state the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Radial Head Prosthesis: Trial Radial Head Elbow joint prosthesis:...

The Issue: The Trial Head may come loose from the implant stem during manipulation of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2013· Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical

Recalled Item: Kerr Maxcem Elite Recalled by Kerr/Pentron, DBA Kerr Corporation and Pentron...

The Issue: Kerr Corporation is initiating this recall because raw material used to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Dimension(R) Phosphorus (PHOS) Flex(R) reagent cartridge (DF61) The...

The Issue: Siemens Healthcare Diagnostics has initiated a voluntary field action for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2013· Bacterin International, Inc.

Recalled Item: OsteoSelect DBM Putty Product Usage: Orthopedic bone filler Recalled by...

The Issue: The firm's retesting procedure was not validated.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Dimension Vista(R) System Vista Drug 4 Calibrator. The device...

The Issue: Siemens has confirmed complaints of low QC and patient recovery with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2013· Bard Access Systems

Recalled Item: Leonard 10.0 French Dual Lumen Catheter with SureCuff Tissue Ingrowth...

The Issue: Bard Access Systems is recalling two lots of Hickman 9.0 French and one lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2013· Bard Access Systems

Recalled Item: Hickman 9.0 French Dual Lumen Catheter with SureCuff Tissue Ingrowth...

The Issue: Bard Access Systems is recalling two lots of Hickman 9.0 French and one lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2013· Orthopedic Alliance LLC

Recalled Item: Femoral component Recalled by Orthopedic Alliance LLC Due to The recall of...

The Issue: The recall of the Loaner Bin and Sterilization Trays for implants and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2013· Orthopedic Alliance LLC

Recalled Item: Tibial baseplate Recalled by Orthopedic Alliance LLC Due to The recall of...

The Issue: The recall of the Loaner Bin and Sterilization Trays for implants and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2013· Orthopedic Alliance LLC

Recalled Item: U2 Acetabular cup Recalled by Orthopedic Alliance LLC Due to The recall of...

The Issue: The recall of the Loaner Bin and Sterilization Trays for implants and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2013· Orthopedic Alliance LLC

Recalled Item: Zweimueller Type Stem SCS-Standard Sz 01 Zweimueller Type Stem SCS-Standard...

The Issue: The recall of the Loaner Bin and Sterilization Trays for implants and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2013· Spinal Solutions, LLC

Recalled Item: Set Screw Recalled by Spinal Solutions, LLC Due to The recall of the Loaner...

The Issue: The recall of the Loaner Bin and Sterilization Trays for implants and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2013· Orthopedic Alliance LLC

Recalled Item: Ball Head Recalled by Orthopedic Alliance LLC Due to The recall of the...

The Issue: The recall of the Loaner Bin and Sterilization Trays for implants and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2013· Spinal Solutions, LLC

Recalled Item: 50 mm Rod Recalled by Spinal Solutions, LLC Due to The recall of the Loaner...

The Issue: The recall of the Loaner Bin and Sterilization Trays for implants and...

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

Class II — Potential Health HazardOngoing