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 2612126140 of 27,451 recalls

Medical DeviceNovember 8, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: ShapeMatch Cutting Guides Product Usage: The ShapeMatch Cutting Guides are...

The Issue: With regards to ShapeMatch Cutting Guides using MRI Imaging, Stryker...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 8, 2012· Medline Industries Inc

Recalled Item: Medline Angio Drape Pack Radiology-LF Recalled by Medline Industries Inc Due...

The Issue: The non-sterile Waste Bag component in the custom pack was attached to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2012· Toshiba American Medical Systems Inc

Recalled Item: Toshiba Infinix-i X-Ray System. A radiographic and fluoroscopic x-ray system...

The Issue: Lost and incorrect images. When using the "F-Rec" fluoroscopy image...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2012· DePuy Spine, Inc.

Recalled Item: DePuy Spine VIPER POLY SCREW 5.5 8 X80MM Tl Product Recalled by DePuy Spine,...

The Issue: Polyaxial screws 8x 80 and larger may disassociate when inserting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2012· IDS (Immunodiagnostic Systems Ltd.)

Recalled Item: 25-Hydroxy Vitamin D EIA Recalled by IDS (Immunodiagnostic Systems Ltd.) Due...

The Issue: Immunodiagnostic Systems is recalling the 25-Hydroxy Vitamin D EIA, AC-57F1...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2012· DePuy Spine, Inc.

Recalled Item: DePuy Spine VIPER POLY SCREW 5.5 9 X 80MM Tl Recalled by DePuy Spine, Inc....

The Issue: Polyaxial screws 8x 80 and larger may disassociate when inserting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2012· DePuy Spine, Inc.

Recalled Item: DePuy Spine VIPER POLY SCREW 5.5 10X100MM Tl Product Code: Recalled by DePuy...

The Issue: Polyaxial screws 8x 80 and larger may disassociate when inserting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2012· DePuy Spine, Inc.

Recalled Item: DePuy Spine VIPER POLY SCREW 5.5 10 X 80MM Tl Recalled by DePuy Spine, Inc....

The Issue: Polyaxial screws 8x 80 and larger may disassociate when inserting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2012· DePuy Spine, Inc.

Recalled Item: DePuy Spine VIPER POLY SCREW 5.5 8 X70MM Tl Product Recalled by DePuy Spine,...

The Issue: Polyaxial screws 8x 80 and larger may disassociate when inserting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2012· DePuy Spine, Inc.

Recalled Item: DePuy Spine VIPER POLY SCREW 5.5 10 X 70MM Tl Recalled by DePuy Spine, Inc....

The Issue: Polyaxial screws 8x 80 and larger may disassociate when inserting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2012· DePuy Spine, Inc.

Recalled Item: DePuy Spine VIPER POLY SCREW 5.5 8 X100MM Tl Product Recalled by DePuy...

The Issue: Polyaxial screws 8x 80 and larger may disassociate when inserting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2012· DePuy Spine, Inc.

Recalled Item: DePuy Spine VIPER POLY SCREW 5.5 9 X70MM Tl Product Recalled by DePuy Spine,...

The Issue: Polyaxial screws 8x 80 and larger may disassociate when inserting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2012· DePuy Spine, Inc.

Recalled Item: DePuy Spine VIPER POLY SCREW 5.5 9 X100MM Tl Product Recalled by DePuy...

The Issue: Polyaxial screws 8x 80 and larger may disassociate when inserting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2012· Invacare Corporation

Recalled Item: Invacare Height Adjustable (walking) Canes Recalled by Invacare Corporation...

The Issue: Following their receipt of several customer complaints, Invacare recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2012· Ethicon Endo-Surgery Inc

Recalled Item: Ethicon Endo-Surgery Inc. The ENSEAL¿ G2 Tissue Sealers are indicated...

The Issue: Potential for self activation while the device is in use, which may result...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2012· Biomet, Inc.

Recalled Item: Echo Bi-Metric Press-Fit Stems/Echo Bi-Metric 11mm x 135mm Collarless Porous...

The Issue: It was reported that the surgeon noticed that the Echo 11mm hip stem had an...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2012· Becton Dickinson & Co.

Recalled Item: BD Phoenix PMIC-108 Panels Recalled by Becton Dickinson & Co. Due to An...

The Issue: An antibiotic susceptibility test kit may produce false intermediate or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2012· Ansell Healthcare Products LLC

Recalled Item: Lifestyles Pleasure Collection 30 Premium Lubricated Condoms Assortment of...

The Issue: One lot of Lifestyles Pleasure Collection Lubricated Condoms is misbranded....

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2012· Arobella Medical, LLC

Recalled Item: Arobella Medical 6mm Qurette used with the Arobella Medical AR1000 Recalled...

The Issue: This recall has been initiated because the Arobella Medical 6mm Qurette Q07...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2012· Medrad Inc

Recalled Item: MEDRAD Hand Controller Sheath Recalled by Medrad Inc Due to The seal between...

The Issue: The seal between the white polyethylene and the clear plastic may be missing...

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

Class II — Potential Health HazardOngoing