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. 2,459 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,459 in last 12 months

Showing 2574125760 of 47,654 recalls

Medical DeviceMarch 13, 2018· Keystone Dental Inc

Recalled Item: Genesis Surgical Cassette Tapered Implants are intended for placement...

The Issue: The surgical cassette contained extra-large white grommets making the 3.8 mm...

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

Class II — Potential Health HazardOngoing
FoodMarch 12, 2018· Food and Beverage Inc.

Recalled Item: Name: Trader Joe s Chocolate Chip Cookies SKU 68075 Net Recalled by Food and...

The Issue: Food & Beverage Inc., dba Chris's Cookies has initiated a recall of Trader...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 12, 2018· Ohio Medical Corporation

Recalled Item: Vacuum Regulator Recalled by Ohio Medical Corporation Due to Final quality...

The Issue: Final quality control testing was not completed before the devices were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· CooperSurgical, Inc.

Recalled Item: 5 mm Apple-Hunt Secondary Cannula/Pyramidal Tip Trocar - extended length...

The Issue: Products have been packaged with the wrong Trocar length type.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Stryker GmbH

Recalled Item: Hinge Coupling Hoffmann LRF Catalog # 4933-0-800 Intended for fixation...

The Issue: The wrong parts were picked for packaging. The connecting Nuts were packed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Stryker Medical Division of Stryker Corporation

Recalled Item: Power-LOAD Cot Fastening System Recalled by Stryker Medical Division of...

The Issue: The power load floor plates which hold the ambulance cot anchors in place...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Zimmer Biomet, Inc.

Recalled Item: Phoenix Nail System Recalled by Zimmer Biomet, Inc. Due to Certain lots of...

The Issue: Certain lots of the Phoenix Tibia Nail 3.5mm Inserter instruments are being...

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

Class II — Potential Health HazardOngoing
DrugMarch 9, 2018· Akorn, Inc.

Recalled Item: Triamcinolone Acetonide Lotion Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: High out of specification...

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

Class III — Low RiskOngoing
Refund
DrugMarch 9, 2018· Alva-Amco Pharmacal Companies., Inc.

Recalled Item: Psoriasin Daytime Relief Cream with Vitamin D & Oatmeal Recalled by...

The Issue: Subpotent Drug: The product has failed to maintain its label claim of coal...

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

Class III — Low RiskOngoing
Refund
DrugMarch 8, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Clocortolone Pivalate Cream Recalled by Dr. Reddy's Laboratories, Inc. Due...

The Issue: Failed Stability Specifications:Out-of-specification results observed for...

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

Class III — Low RiskOngoing
Refund
DrugMarch 7, 2018· American Pharmaceutical Ingredients LLC

Recalled Item: Oxytocin USP Recalled by American Pharmaceutical Ingredients LLC Due to...

The Issue: Stability Data Does Not Support Expiry: Stability data from manufacturer...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 7, 2018· American Pharmaceutical Ingredients LLC

Recalled Item: Sermorelin Acetate Recalled by American Pharmaceutical Ingredients LLC Due...

The Issue: Stability Data Does Not Support Expiry: Stability data from manufacturer...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 7, 2018· Intuitive Surgical, Inc.

Recalled Item: da Vinci X Surgical System Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Specific da Vinci X Surgical Systems (IS4200) were shipped with defective...

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

Class II — Potential Health HazardOngoing
FoodMarch 6, 2018· Piggie Park Enterprises Inc

Recalled Item: Maurice's Honey Southern Gold BBQ Sauce Recalled by Piggie Park Enterprises...

The Issue: Undeclared soy and wheat ingredients

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 5, 2018· Johnson Matthey Inc.

Recalled Item: Morphine Sulfate USP Milled Recalled by Johnson Matthey Inc. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: Bioburden out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 5, 2018· InvaGen Pharmaceuticals, Inc.

Recalled Item: Decitabine for Injection Recalled by InvaGen Pharmaceuticals, Inc. Due to...

The Issue: Failed impurities/degradation specifications: Failure to water content and...

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

Class III — Low RiskOngoing
Refund
DrugMarch 5, 2018· Novel Laboratories, Inc.

Recalled Item: Lupin Hydrocodone Bitartrate and Homatropine Methylbromide Tablets Recalled...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugMarch 5, 2018· Sagent Pharmaceuticals Inc

Recalled Item: methylPREDNISolone Sodium Succinate for Injection Recalled by Sagent...

The Issue: Failed Impurities/Degradation Specifications: High out of specification...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 5, 2018· Sagent Pharmaceuticals Inc

Recalled Item: methylPREDNISolone Sodium Succinate for Injection Recalled by Sagent...

The Issue: Failed Impurities/Degradation Specifications: High out of specification...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 5, 2018· Sagent Pharmaceuticals Inc

Recalled Item: methylPREDNISolone Sodium Succinate for Injection Recalled by Sagent...

The Issue: Failed Impurities/Degradation Specifications: High out of specification...

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

Class II — Potential Health HazardOngoing
Refund