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. 2,360 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,360 in last 12 months

Showing 4722147240 of 47,654 recalls

Medical DeviceMarch 29, 2012· The Anspach Effort, Inc.

Recalled Item: MCA5-1SB - 1MM Fluted Ball Recalled by The Anspach Effort, Inc. Due to The...

The Issue: The Anspach Effort, Inc. is recalling all lots of the Anspach Micro Curved...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2012· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius GranuFlo (powder) Acid Concentrate Product Codes: OFD1201-3B...

The Issue: Risk of Alkalosis with acetate containing dialysis acid concentrates

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 29, 2012· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius NaturaLyte Liquid Acid Concentrate Product Codes: 08-0231-4...

The Issue: Risk of Alkalosis with acetate containing dialysis acid concentrates

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 27, 2012· Nidek Inc

Recalled Item: MC-500 Multicolor Laser Photocoagulator Recalled by Nidek Inc Due to The...

The Issue: The spot size control of the scan delivery unit of the MC-500 Multicolor...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2012· B. Braun Medical, Inc.

Recalled Item: Space Pump Pole Clamps for the Infusomat Space Pump Recalled by B. Braun...

The Issue: Firm has become aware of the potential for breakage of the pole clamp...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2012· B. Braun Medical, Inc.

Recalled Item: Infusomat(R) Space Pump (US Version) with software version 686G030103...

The Issue: Firm became aware of the potential for breakage of the anti free flow clip...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 23, 2012· Colgate Palmolive Company

Recalled Item: Colgate 360 Replaceable Head Battery Powered Bonus Twin Pack Toothbrush...

The Issue: Brush battery cap was forcibly blown off at the end of the brush handle.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2012· Colgate Palmolive Company

Recalled Item: Colgate Adult Motion Battery Toothbrush Dist. by Colgate-Palmolive Recalled...

The Issue: Brush battery cap was forcibly blown off at the end of the brush handle.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2012· Colgate Palmolive Company

Recalled Item: Colgate 360 Replaceable Head Battery Powered Toothbrush Soft Recalled by...

The Issue: Brush battery cap was forcibly blown off at the end of the brush handle.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2012· Colgate Palmolive Company

Recalled Item: Colgate 360 Replaceable Head Battery Powered Toothbrush Medium Dist....

The Issue: Brush battery cap was forcibly blown off at the end of the brush handle.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2012· Colgate Palmolive Company

Recalled Item: Colgate Adult Motion Whitening Battery Toothbrush Dist. by Recalled by...

The Issue: Brush battery cap was forcibly blown off at the end of the brush handle.

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

Class II — Potential Health HazardOngoing
DrugMarch 22, 2012· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (Methylphenidate) Transdermal System Patch Recalled by Noven...

The Issue: Miscalibrated/Defective Delivery System; exceeded the specification for both...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 22, 2012· Extremity Medical LLC

Recalled Item: Extremity Medical Recalled by Extremity Medical LLC Due to Lag screw...

The Issue: Lag screw measurement is short (approximately 5 mm) when using current screw...

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

Class II — Potential Health HazardOngoing
DrugMarch 16, 2012· Ranbaxy Inc.

Recalled Item: Balnetar Therapeutic Tar Bath Recalled by Ranbaxy Inc. Due to Subpotent...

The Issue: Subpotent (Single Ingredient Drug): out-of-specification result for coal tar...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 15, 2012· Sunquest Information Systems, Inc.

Recalled Item: Sunquest Laboratory Sunquest Laboratory is intended for use by professionals...

The Issue: Sunquest is recalling Sunquest Laboratory versions 6.1.0125 through...

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

Class II — Potential Health HazardOngoing
DrugMarch 14, 2012· Zydus Pharmaceuticals USA Inc

Recalled Item: Metformin Hydrochloride Tablets Recalled by Zydus Pharmaceuticals USA Inc...

The Issue: Presence of Foreign Substance(s): A product complaint was received from a...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 13, 2012· Advanced Sterilization Products

Recalled Item: STERRAD 200 System Carriage Recalled by Advanced Sterilization Products Due...

The Issue: Advanced Sterilization Products (ASP) is recalling the STERRAD 200 System...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: DePuy Mitek VAPR Hook Electrode 3.5mm Hook Electrode with Integrated...

The Issue: Product may have wrong large product identification label with symbols on...

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

Class II — Potential Health HazardOngoing
DrugMarch 9, 2012· Aurobindo Pharma LTD

Recalled Item: Northstar Zolpidem Tartrate Tablets USP 10 mg. Manufactured for Northstar RX...

The Issue: Adulterated Presence of Foreign Tablets: This product is being recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 9, 2012· Pack Pharmaceuticals

Recalled Item: Ciprofloxacin Tablets Recalled by Pack Pharmaceuticals Due to Labeling...

The Issue: Labeling Illegible: Missing Label; The voluntary recall of the...

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

Class III — Low RiskOngoing
Refund