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. 2,366 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,366 in last 12 months

Showing 4530145320 of 47,654 recalls

Medical DeviceNovember 29, 2012· Thermo Fisher Scientific (Asheville) LLC

Recalled Item: CO2 Incubators (General Purpose Incubator) Recalled by Thermo Fisher...

The Issue: Incubators manufactured prior to mid 2009 have coated metal hinges that have...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 28, 2012· Philips Healthcare Inc.

Recalled Item: Mobile Diagnostic X-Ray System with Digital Panel Recalled by Philips...

The Issue: When the operator moves an image to another view then the electronic marker...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 28, 2012· Beckman Coulter Inc.

Recalled Item: Beckman Coulter AU5800 Clinical Chemistry Analyzer. An automated chemistry...

The Issue: Due to a software data storage limitation which only occurs under certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 28, 2012· Mindray DS USA, Inc. d.b.a. Mindray North America

Recalled Item: Mindray DS USA Recalled by Mindray DS USA, Inc. d.b.a. Mindray North America...

The Issue: Mindray has identified a software anomaly that may where, in the presence of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 28, 2012· DePuy Orthopaedics, Inc.

Recalled Item: Pinnacle Cancellous Screw Packaging: Product is housed within a polyurethane...

The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary recall of ten lots of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2012· Radiometer America Inc

Recalled Item: TCM4 series Base Units Recalled by Radiometer America Inc Due to RADIOMETER...

The Issue: RADIOMETER became aware that the TCM4 series Base Unit does not comply with...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Dimension(R) Tacrolimus Flex(R) reagent cartridge (DF107). The TACR...

The Issue: Siemens has confirmed customer complaints of low patient sample recovery...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2012· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Somatom CTs equipped with software syngo CT2010A Recalled by Siemens...

The Issue: Sporadic hang-up malfunctions concerning 3D reconstructions during activated...

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

Class II — Potential Health HazardOngoing
DrugNovember 26, 2012· Pfizer Inc.

Recalled Item: TORISEL Kit (temsirolimus) injection Recalled by Pfizer Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility; potential that a low level of endotoxins may...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 26, 2012· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius GranuFlo Dry Acid Concentrate For Bicarbonate Dialysis 2.0 K...

The Issue: GranuFlo Dry Acid Concentrate may show discoloration

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

Class III — Low RiskOngoing
Medical DeviceNovember 26, 2012· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Axiom Artis zeego systems with software version VC14 Recalled by...

The Issue: In the course of the firm's product monitoring activities, a potential risk...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2012· Custom Healthcare Systems, Inc.

Recalled Item: Custom Breast Biopsy Tray w/Sodium Chloride Recalled by Custom Healthcare...

The Issue: Surgical procedure trays are packed with pharmaceuticals for injection that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2012· Custom Healthcare Systems, Inc.

Recalled Item: Custom Breast Biopsy Tray Recalled by Custom Healthcare Systems, Inc. Due to...

The Issue: Surgical procedure trays are packed with pharmaceuticals for injection that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2012· Perkinelmer

Recalled Item: DBS MICROPLATE Recalled by Perkinelmer Due to Truncated V-Bottomed...

The Issue: Truncated V-Bottomed Microplate Wells used in assays contain defective wells.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2012· Perkinelmer

Recalled Item: NEONATAL TOTAL GALACTOSE KIT Product Numbers: 3029-0010 Recalled by...

The Issue: Truncated V-Bottomed Microplate Wells used in assays contain defective wells.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2012· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius GranuFlo Naturalyte Dry Acid Concentrate For Bicarbonate Dialysis...

The Issue: GranuFlo Dry Acid Concentrate may show discoloration

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

Class III — Low RiskOngoing
Medical DeviceNovember 26, 2012· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius GranuFlo Naturalyte Dry Acid Concentrate For Bicarbonate Dialysis...

The Issue: GranuFlo Dry Acid Concentrate may show discoloration

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

Class III — Low RiskOngoing
Medical DeviceNovember 26, 2012· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius GranuFlo Naturalyte Dry Acid Concentrate For Bicarbonate Dialysis...

The Issue: GranuFlo Dry Acid Concentrate may show discoloration

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

Class III — Low RiskOngoing
Medical DeviceNovember 26, 2012· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius GranuFlo Naturalyte Dry Acid Concentrate For Bicarbonate Dialysis...

The Issue: GranuFlo Dry Acid Concentrate may show discoloration

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

Class III — Low RiskOngoing
Medical DeviceNovember 26, 2012· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius GranuFlo Naturalyte Dry Acid Concentrate For Bicarbonate Dialysis...

The Issue: GranuFlo Dry Acid Concentrate may show discoloration

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

Class III — Low RiskOngoing