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. 938 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
938 in last 12 months

Showing 36681–36700 of 47,654 recalls

Medical DeviceMay 1, 2015· Beaver-Visitec International Inc.

Recalled Item: BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon...

The Issue: Devon Light Glove in procedure kits may have holes/slits compromising...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2015· Beaver-Visitec International Inc.

Recalled Item: BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon...

The Issue: Devon Light Glove in procedure kits may have holes/slits compromising...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2015· Integra LifeSciences Corp. d.b.a. Integra Pain Management

Recalled Item: Integra¿ Long Epidural Steroid Injection Needle (Tuohy Needle) Recalled by...

The Issue: Integra LifeSciences Corp. d.b.a. Integra Pain Management Announces...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2015· Biomet, Inc.

Recalled Item: Unilateral external fixation ankle clamp Product Usage: Unilateral external...

The Issue: Ankle clamp was assembled incorrectly; the offset of the pin to the pivot...

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

Class II — Potential Health HazardOngoing
FoodMay 1, 2015· Poco Dolce Confections, Inc.

Recalled Item: Poco Dolce Bittersweet Chocolate: Almond Tile Recalled by Poco Dolce...

The Issue: California Department of Public Health conducted and inspection of the firm...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 1, 2015· Poco Dolce Confections, Inc.

Recalled Item: Poco Dolce Bittersweet Chocolate: Almond Coconut Tile Recalled by Poco Dolce...

The Issue: California Department of Public Health conducted and inspection of the firm...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 1, 2015· Poco Dolce Confections, Inc.

Recalled Item: Poco Dolce Bittersweet Chocolate: Burnt Caramel Tile Recalled by Poco Dolce...

The Issue: California Department of Public Health conducted and inspection of the firm...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 1, 2015· Poco Dolce Confections, Inc.

Recalled Item: Poco Dolce Bittersweet Chocolate: Sesame Toffee Tile Recalled by Poco Dolce...

The Issue: California Department of Public Health conducted and inspection of the firm...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 1, 2015· Poco Dolce Confections, Inc.

Recalled Item: Poco Dolce Bittersweet Chocolate: Ginger Tile Recalled by Poco Dolce...

The Issue: California Department of Public Health conducted and inspection of the firm...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 1, 2015· Poco Dolce Confections, Inc.

Recalled Item: Poco Dolce Bittersweet Chocolate: Aztec Chili Tile Recalled by Poco Dolce...

The Issue: California Department of Public Health conducted and inspection of the firm...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 30, 2015· Zimmer, Inc.

Recalled Item: PRI Femoral Impactor Block for knee prosthesis surgery. Orthopedic Manual...

The Issue: Potential for uncured adhesive between the metal threaded insert and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2015· Neuro Kinetics, Inc.

Recalled Item: I-Portal¿ NOTC and VNG Recalled by Neuro Kinetics, Inc. Due to complaints of...

The Issue: complaints of system malfunction and unintended, sudden movement at start...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2015· Smith & Nephew, Inc.

Recalled Item: ULTRA-FAST FIX Knot Pusher Suture Cutters Product Number: 72201537 Intended...

The Issue: Sterility of device maybe compromised

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

Class II — Potential Health HazardOngoing
DrugApril 30, 2015· Mission Pharmacal Co

Recalled Item: Sodium Sulfacetamide 9% and Sulfur 4.5% Wash Kit Recalled by Mission...

The Issue: Microbial Contamination of Non-Sterile Products: Product failed USP...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 30, 2015· Mission Pharmacal Co

Recalled Item: Sodium Sulfacetamide 9% and Sulfur 4.5% Wash Kit with Sunscreen Recalled by...

The Issue: Microbial Contamination of Non-Sterile Products: Product failed USP...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 29, 2015· Janssen Pharmaceuticals, Inc.

Recalled Item: Ortho-Cept (0.15 mg desogestrel and 0.03 mg ethinyl estradiol) tablets...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 29, 2015· Richard-Allan Scientific Company

Recalled Item: Mucolytic Agent 1 pint/473 ml Recalled by Richard-Allan Scientific Company...

The Issue: Richard Allan Scientific (RAS) is initiating a recall of Mucolytic agent and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2015· HeartWare Inc

Recalled Item: HeartWare Ventricular Assist System (HVAD). Catalog #'s US: 1101 and...

The Issue: Complaints with the HVAD Internal Controller Alarm Battery failures.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 29, 2015· Zimmer, Inc.

Recalled Item: Cortical Screw for M/DN Intramedullary Fixation. Metaphyseal/Diaphyseal Nail...

The Issue: The entire scope of 4.5mm Cortical Screws listed as compatible with the M/DN...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2015· HeartWare Inc

Recalled Item: HeartWare Ventricular Assist System (HVAD) For use as a bridge-to-cardiac...

The Issue: Complaints with the HVAD Discolored and Cracked Driveline Outer Sheath.

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

Class II — Potential Health HazardOngoing