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 4544145460 of 47,654 recalls

FoodNovember 7, 2012· Reaction Nutrition LLC

Recalled Item: Clinical LIVE Dietary Supplement Immune Support 694.325 mg 90 capsules...

The Issue: The product contained an undeclared allergen, Colostrum, which is considered...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
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· 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 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 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 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 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 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 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 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· 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
DrugNovember 6, 2012· Alkermes, Inc.

Recalled Item: VIVITROL (naltrexone for extended-release injectable suspension) a) 380 mg...

The Issue: Lack of Assurance of Sterility: Product did not meet the criteria for...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 6, 2012· Omya Inc

Recalled Item: Ground limestone also known as calcium carbonate. Omya's food grade Recalled...

The Issue: Omya Inc. is voluntarily recalling certain lots of food grade ground...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
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· 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· 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 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
DrugNovember 5, 2012· Caraco Pharmaceutical Laboratories, Ltd.

Recalled Item: traMADOL Hydrochloride Tablets Recalled by Caraco Pharmaceutical...

The Issue: Adulterated Presence of Foreign Tablets: A customer complaint was received...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 5, 2012· Boehringer Ingelheim Roxane Inc

Recalled Item: Pradaxa (dabigatran etexilate) Recalled by Boehringer Ingelheim Roxane Inc...

The Issue: Defective container; damaged bottles could allow moisture to get into the...

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

Class II — Potential Health HazardOngoing
Refund
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