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 2658126600 of 27,451 recalls

Medical DeviceJuly 24, 2012· DePuy Spine, Inc.

Recalled Item: DePuy Spine EXPEDIUM Offset Torque Wrench Product Code 2797-29-510 The...

The Issue: A component within the handle of the Expedium Offset Torque Wrench is...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2012· Beckman Coulter Inc.

Recalled Item: Access Folate Calibrators Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter is recalling the Access Folate Calibrators because it may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2012· Beckman Coulter Inc.

Recalled Item: Access Folate WHO Calibrators Recalled by Beckman Coulter Inc. Due to...

The Issue: Beckman Coulter is recalling the Access Folate Calibrators because it may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2012· Cisco Systems Inc

Recalled Item: Cisco brand HealthPresence Recalled by Cisco Systems Inc Due to Software...

The Issue: Software anomaly may result in incorrect values and interpretations. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2012· Galil Medical, Inc.

Recalled Item: Visual-ICE¿ Cryoablation System Recalled by Galil Medical, Inc. Due to Galil...

The Issue: Galil Medical is recalling a number of Visual Ice Cryoablation Systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2012· GE Healthcare, LLC

Recalled Item: CARESCAPE Monitor B850 Product Usage: The CARESCAPE TM Monitor B850 Recalled...

The Issue: GE Healthcare become aware of 4 potential issues associated with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2012· Abbott Point Of Care Inc.

Recalled Item: Cliniqa Liquid QCTM Cardiac Marker Control for i-STAT Level 1 Recalled by...

The Issue: Abbott Point of Care (APOC) has determined that for the Cliniqa Liquid QC...

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

Class III — Low RiskOngoing
Medical DeviceJuly 18, 2012· Zimmer, Inc.

Recalled Item: 00-4309-028-01 - Trabecular Metal Reverse Shoulder Liner 40mm 65¿ Neck...

The Issue: Lot specific Trabecular Metal (TM) Reverse Shoulder Liner Impactors are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2012· Nellcor Puritan Bennett Inc. (dba Covidien LP)

Recalled Item: Shiley Reusable Cannula Low Pressure Cuffed Tracheostomy Tubes Recalled by...

The Issue: Covidien is recalling certain cuffed Shiley tracheostomy tubes due to...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 18, 2012· Zimmer, Inc.

Recalled Item: 00-4309-029-01 - Trabecular Metal Reverse Shoulder Liner 36 mm 65¿¿ Recalled...

The Issue: Lot specific Trabecular Metal (TM) Reverse Shoulder Liner Impactors are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2012· Zimmer, Inc.

Recalled Item: Trabecular Metal Reverse Shoulder Liner 40mm Recalled by Zimmer, Inc. Due to...

The Issue: Lot specific Trabecular Metal (TM) Reverse Shoulder Liner Impactors are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2012· Zimmer, Inc.

Recalled Item: 00-4309-029-00- Trabecular Metal Reverse Shoulder Liner 36mm Recalled by...

The Issue: Lot specific Trabecular Metal (TM) Reverse Shoulder Liner Impactors are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2012· Siemens Medical Solutions USA, Inc

Recalled Item: syngo Imaging XS. Radiological image processing system. Recalled by Siemens...

The Issue: There is a potential malfunction when using syngo Imaging XS, version VA70A...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2012· Siemens Medical Solutions USA, Inc

Recalled Item: syngo.plaza Recalled by Siemens Medical Solutions USA, Inc Due to There is a...

The Issue: There is a potential malfunction in which a miscalculation occurs for images...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur¿ Syphilis (SYPH) Assay Recalled by Siemens Healthcare...

The Issue: Syphilis Assay Interference with HBsAg Assay

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2012· Stryker Instruments Div. of Stryker Corporation

Recalled Item: RF Cannula Recalled by Stryker Instruments Div. of Stryker Corporation Due...

The Issue: Stryker has received 6 complaints that the 5mm needle was placed in 10 mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension(R) Reagent Management System (RMS) - Power Cord. The Siemens...

The Issue: Siemens Healthcare Diagnostics has confirmed that partial insertion of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2012· Stryker Instruments Div. of Stryker Corporation

Recalled Item: RF Cannula Recalled by Stryker Instruments Div. of Stryker Corporation Due...

The Issue: Stryker has received 6 complaints that the 5mm needle was placed in 10 mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista(R) Vancomycin Flex(R) Reagent Cartridge (VANC Recalled by...

The Issue: Siemens has received complaints of customers experiencing slopes >1.05 when...

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

Class III — Low RiskOngoing
Medical DeviceJuly 17, 2012· Conformis Inc

Recalled Item: Conformis iTotal CR-Cruciate Retaining Knee Replacement System Model...

The Issue: Addendum Labeling iTotal CR Surgical Technique with Detailed Instructions of...

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

Class II — Potential Health HazardOngoing