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 3024130260 of 47,654 recalls

FoodDecember 7, 2016· All American Seasonings, Inc.

Recalled Item: Jalapeno Popper ASI. Product Code: T3934. 33 lb bags Recalled by All...

The Issue: Products have been recalled due to potential for Salmonella contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 7, 2016· All American Seasonings, Inc.

Recalled Item: Super Nacho (No-Pho Recalled by All American Seasonings, Inc. Due to...

The Issue: Products have been recalled due to potential for Salmonella contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 7, 2016· All American Seasonings, Inc.

Recalled Item: OC Ranch French Fry Seasoning/CraftWorks. Product Code: T3996. 12 lb bags...

The Issue: Products have been recalled due to potential for Salmonella contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 7, 2016· All American Seasonings, Inc.

Recalled Item: Habanero Ranch Seasoning / Shearer's. Product Code: T4053. 50 lb bags...

The Issue: Products have been recalled due to potential for Salmonella contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 7, 2016· All American Seasonings, Inc.

Recalled Item: FH Parmesan. Product Code: T206486-50. 50 lb bags Recalled by All American...

The Issue: Products have been recalled due to potential for Salmonella contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 7, 2016· All American Seasonings, Inc.

Recalled Item: Xtra Sharp Cheese Sauce. Product Code: T4015. 37.5 lb bags Recalled by All...

The Issue: Products have been recalled due to potential for Salmonella contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 7, 2016· All American Seasonings, Inc.

Recalled Item: Chipotle Ranch ASI. Product Code: T3883. 33 lb bags Recalled by All American...

The Issue: Products have been recalled due to potential for Salmonella contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 7, 2016· All American Seasonings, Inc.

Recalled Item: French Onion Seasoning ASI. Product Code: T3933. 33 lb bags Recalled by All...

The Issue: Products have been recalled due to potential for Salmonella contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 7, 2016· Cargill Cocoa & Chocolate, Inc.

Recalled Item: Wilbur Recalled by Cargill Cocoa & Chocolate, Inc. Due to Undeclared Milk

The Issue: Cargill Cocoa & Chocolate is recalling 50 lb. cartons of Wilbur B558...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 7, 2016· Stanmore Implants Worldwide Ltd.

Recalled Item: Tibial Component Fixed Hinge Small Long Recalled by Stanmore Implants...

The Issue: The recalling firm has received 5 customer inquiries reporting that at least...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2016· Stanmore Implants Worldwide Ltd.

Recalled Item: Femoral Shaft L=120mm Recalled by Stanmore Implants Worldwide Ltd. Due to...

The Issue: The recalling firm has received 5 customer inquiries reporting that at least...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2016· Stanmore Implants Worldwide Ltd.

Recalled Item: DF Coated Integral Shaft & Stem 15x30x38 Recalled by Stanmore Implants...

The Issue: The recalling firm has received 5 customer inquiries reporting that at least...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2016· Stanmore Implants Worldwide Ltd.

Recalled Item: Tibial Component Metal Cased Small Long Recalled by Stanmore Implants...

The Issue: The recalling firm has received 5 customer inquiries reporting that at least...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2016· Stanmore Implants Worldwide Ltd.

Recalled Item: Femoral Integral Shaft & Stem 15x27 HA Coated Recalled by Stanmore Implants...

The Issue: The recalling firm has received 5 customer inquiries reporting that at least...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2016· Cardiovascular Systems Inc

Recalled Item: DIAMONDBACK 360 Peripheral 1.50 Classic Recalled by Cardiovascular Systems...

The Issue: CSI discovered that a 1.50mm Solid Crown OAD was labeled as a 1.50mm Crown OED.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2016· Medacta Usa Inc

Recalled Item: Medacta International SA Recalled by Medacta Usa Inc Due to Damaged...

The Issue: Damaged packaging, lack of sterility assurance

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

Class II — Potential Health HazardOngoing
DrugDecember 7, 2016· Novum Pharma, LLC

Recalled Item: Novacort Gel Sample Packets (2% hydrocortisone acetate Recalled by Novum...

The Issue: Subpotent Drug: Out of specification result for pramoxine hydrochloride

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 6, 2016· Stryker Sustainability Solutions

Recalled Item: Reprocessed Ablation Catheter Cable Catalog Number: CR3425CT Recalled by...

The Issue: A breach in the sterile packaging may have occurred resulting in potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2016· Accuray Incorporated

Recalled Item: CyberKnife Robotic Radiosurgery Systems Recalled by Accuray Incorporated Due...

The Issue: Accuray has become aware of a potential safety issue involving the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2016· Stryker Sustainability Solutions

Recalled Item: Reprocessed Electrophysiology Catheter Cables Catalog Number: CB3434CT...

The Issue: A breach in the sterile packaging may have occurred resulting in potentially...

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

Class II — Potential Health HazardOngoing