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 4704147060 of 47,654 recalls

Medical DeviceMay 9, 2012· Covidien LP

Recalled Item: Covidien ROTICULATOR 30-4.8 Single Use Stapler REF# 017617 The RETICULA...

The Issue: Potential for the sterility barrier to be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: SPECIALTYCARE - HUDGENS. The Sarns High Flow Aortic Arch Cannula Recalled by...

The Issue: During production of one lot of the Sarns High-Flow Aortic Arch Cannula,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Covidien LP

Recalled Item: Covidien ROTICULATOR 30-V3 Single Use Stapler REF# 017619 The RETICULA...

The Issue: Potential for the sterility barrier to be compromised.

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

Class II — Potential Health HazardOngoing
DrugMay 8, 2012· Morton Salt Co.

Recalled Item: Morton Recalled by Morton Salt Co. Due to Impurities/Degradation Products:...

The Issue: Impurities/Degradation Products: The product was found to contain a slightly...

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

Class III — Low RiskOngoing
Refund
DrugMay 8, 2012· Hill Dermaceuticals, Inc.

Recalled Item: Derma-Smoothe/FS (Fluocinolone Acetonide) 0.01% Topical Oil (Scalp Oil)...

The Issue: Subpotent; fluocinolone acetonide

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

Class III — Low RiskOngoing
Refund
DrugMay 8, 2012· Hill Dermaceuticals, Inc.

Recalled Item: Derma-Smoothe/FS (Fluocinolone Acetonide) 0.01% Recalled by Hill...

The Issue: Subpotent; fluocinolone acetonide

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

Class III — Low RiskOngoing
Refund
FoodMay 8, 2012· Seoul Shik Poom, Inc.

Recalled Item: Frozen Oysters Recalled by Seoul Shik Poom, Inc. Due to Korean Certified...

The Issue: Korean Certified Shippers delisted from ICSSL.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 8, 2012· Seoul Shik Poom, Inc.

Recalled Item: Frozen Salted Clam Recalled by Seoul Shik Poom, Inc. Due to Korean Certified...

The Issue: Korean Certified Shippers delisted from ICSSL.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 8, 2012· Panera Bread LLC

Recalled Item: Panera Recalled by Panera Bread LLC Due to Product ingredient statement...

The Issue: Product ingredient statement reversed for Reduced Fat Honey Walnut Cream...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 8, 2012· Panera Bread LLC

Recalled Item: Panera HONEY WALNUT CREAM CHEESE SPREAD Recalled by Panera Bread LLC Due to...

The Issue: Product ingredient statement reversed for Reduced Fat Honey Walnut Cream...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 8, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Dimension Vista(R) System B12 Flex(R) Reagent Cartridge (K6442) B12...

The Issue: Siemens Healthcare Diagnostics has confirmed that the presence of Intrinsic...

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

Class II — Potential Health HazardOngoing
DrugMay 7, 2012· Guthy-Renker LLC

Recalled Item: Rodan & Fields Proactiv Solution Recalled by Guthy-Renker LLC Due to...

The Issue: Subpotent Drug: Salicylic acid is subpotent.

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

Class III — Low RiskOngoing
Refund
DrugMay 7, 2012· Guthy-Renker LLC

Recalled Item: Rodan & Fields Proactiv Solution Recalled by Guthy-Renker LLC Due to...

The Issue: Subpotent Drug: Salicylic acid is subpotent.

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

Class III — Low RiskOngoing
Refund
DrugMay 7, 2012· Guthy-Renker LLC

Recalled Item: Rodan & Fields Proactiv Solution Recalled by Guthy-Renker LLC Due to...

The Issue: Subpotent Drug: Salicylic acid is subpotent.

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

Class III — Low RiskOngoing
Refund
DrugMay 7, 2012· Guthy-Renker LLC

Recalled Item: Rodan & Fields Proactiv Solution Recalled by Guthy-Renker LLC Due to...

The Issue: Subpotent Drug: Salicylic acid is subpotent.

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

Class III — Low RiskOngoing
Refund
DrugMay 7, 2012· Guthy-Renker LLC

Recalled Item: Rodan & Fields Proactiv Solution Recalled by Guthy-Renker LLC Due to...

The Issue: Subpotent Drug: Salicylic acid is subpotent.

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

Class III — Low RiskOngoing
Refund
DrugMay 7, 2012· Endo Pharmaceuticals, Inc.

Recalled Item: Endocet (oxycodone and acetaminophen) tablets Recalled by Endo...

The Issue: Adulterated Presence of Foreign Tablets: Customer complaint that some...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 7, 2012· MTI Precision Products LLC.

Recalled Item: Lynx TM20 Torquemaster Low Speed Handpiece MTI Dental Products Recalled by...

The Issue: Sharp edge on the body/housing of the Lynx TM20 TorqueMaster Low Speed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2012· Mindray DS USA, Inc. d.b.a. Mindray North America

Recalled Item: V Series Patient Monitors Recalled by Mindray DS USA, Inc. d.b.a. Mindray...

The Issue: Mindray has identified two software anomalies contained in the V Series...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2012· JK Products & Services, Inc

Recalled Item: BeautyAngel Health Fitness Natural Collagen Stimulation Anti Aging For human...

The Issue: The Beauty Angel was marketed without a 510k.

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

Class II — Potential Health HazardOngoing