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 2964129660 of 47,654 recalls

FoodFebruary 24, 2017· Manzana Products Co., Inc.

Recalled Item: Trader Joe's Organic Unsweetened Apple Sauce Recalled by Manzana Products...

The Issue: Manzana Products Co. is initiating a recall of three varieties of apple...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 24, 2017· Manzana Products Co., Inc.

Recalled Item: Trader Joe's All Natural Unsweetened Apple Sauce Recalled by Manzana...

The Issue: Manzana Products Co. is initiating a recall of three varieties of apple...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 24, 2017· Trader Joes Company

Recalled Item: Trader Joes Imported English Authentic Lemon Curd Recalled by Trader Joes...

The Issue: Trader Joe's Co. is recalling the Lemon Curd because it contains undeclared...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 24, 2017· Philips North America, LLC

Recalled Item: HeartStart MRx Monitor/Defibrillator Recalled by Philips North America, LLC...

The Issue: HeartStart MRx Monitor/Defibrillator may may exhibit abnormal behavior when...

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

Class I — Serious Health HazardOngoing
DrugFebruary 23, 2017· Mckesson Packaging Services

Recalled Item: Aspirin Chewable Tablets Recalled by Mckesson Packaging Services Due to...

The Issue: Presence of Foreign Substance: foreign material found in the bulk inventory.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 23, 2017· Carefusion 2200 Inc

Recalled Item: JAMSHIDI NEEDLE BIOPSY [15G X 100MM DISP Recalled by Carefusion 2200 Inc Due...

The Issue: The integrity of the sterile packaging is potentially compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Carefusion 2200 Inc

Recalled Item: Thoracentesis/ Paracentesis Kit 10/CS Recalled by Carefusion 2200 Inc Due to...

The Issue: The integrity of the sterile packaging is potentially compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Carefusion 2200 Inc

Recalled Item: JAMSHIDI (TJ) NEEDLE BM ASP MAC [a.) 13G x 3.5 Recalled by Carefusion 2200...

The Issue: The integrity of the sterile packaging is potentially compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Carefusion 2200 Inc

Recalled Item: ILLINOIS (TJ) NEEDLE ASPIRATION [15GA Recalled by Carefusion 2200 Inc Due to...

The Issue: The integrity of the sterile packaging is potentially compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Carefusion 2200 Inc

Recalled Item: Manometer Recalled by Carefusion 2200 Inc Due to The integrity of the...

The Issue: The integrity of the sterile packaging is potentially compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Carefusion 2200 Inc

Recalled Item: JAMSHIDI (TJ) NEEDLE BONE MARROW [a.) 13G x 3.5 Recalled by Carefusion 2200...

The Issue: The integrity of the sterile packaging is potentially compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Hill-Rom, Inc.

Recalled Item: TotalCare Bed Systems Recalled by Hill-Rom, Inc. Due to The bed exit alarm...

The Issue: The bed exit alarm may not function properly if the alarm has been armed for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Enzyme 2 Calibrator Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics has confirmed a positive bias of up to 41% in...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 23, 2017· Streck

Recalled Item: Cyto-Chex BCT - blood specimen collection device - Immunophenotyping...

The Issue: Complaints of the 2.0ml tube stopper coming loose during phlebotomy when...

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

Class II — Potential Health HazardOngoing
DrugFebruary 22, 2017· Advanced Pharma Inc.

Recalled Item: Atropine Sulfate all strengths Recalled by Advanced Pharma Inc. Due to...

The Issue: Labeling: Not Elsewhere Classified: Products may contain synthetic latex...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 22, 2017· Advanced Pharma Inc.

Recalled Item: Esmolol HCl all strengths Recalled by Advanced Pharma Inc. Due to Labeling:...

The Issue: Labeling: Not Elsewhere Classified: Products may contain synthetic latex...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 22, 2017· Advanced Pharma Inc.

Recalled Item: Neostigmine Methylsulfate all strengths Recalled by Advanced Pharma Inc. Due...

The Issue: Labeling: Not Elsewhere Classified: Products may contain synthetic latex...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 22, 2017· Advanced Pharma Inc.

Recalled Item: Meperidine HCl all strengths Recalled by Advanced Pharma Inc. Due to...

The Issue: Labeling: Not Elsewhere Classified: Products may contain synthetic latex...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 22, 2017· Advanced Pharma Inc.

Recalled Item: Midazolam HCl all strengths Recalled by Advanced Pharma Inc. Due to...

The Issue: Labeling: Not Elsewhere Classified: Products may contain synthetic latex...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 22, 2017· Advanced Pharma Inc.

Recalled Item: Fentanyl Citrate all strengths Recalled by Advanced Pharma Inc. Due to...

The Issue: Labeling: Not Elsewhere Classified: Products may contain synthetic latex...

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

Class II — Potential Health HazardOngoing
Refund