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. 1,737 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
1,737 in last 12 months

Showing 3262132640 of 47,654 recalls

Medical DeviceApril 22, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH SYS 64-3R to 64-4R Recalled by Siemens Medical Solutions USA Inc....

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH 64 - 3 Ring Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH 40 - 3 Ring Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH mCT Flow 64-3R Recalled by Siemens Medical Solutions USA Inc. Due...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...

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

Class II — Potential Health HazardOngoing
DrugApril 22, 2016· Dr. Reddy's Laboratories, Inc.

Recalled Item: CVS pharmacy Original Strength Acid Controller tablets Recalled by Dr....

The Issue: Failed impurities/degradation specification: An out of specification results...

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 21, 2016· Musculoskeletal Transplant Foundation, Inc.

Recalled Item: Musculoskeletal Transplant Foundation Recalled by Musculoskeletal Transplant...

The Issue: AFT Diverted Tubes are being recalled due to a customer complaint involving...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2016· Baxter Healthcare Corp.

Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...

The Issue: Instructions for use booklet may puncture the outer Tyvek lid.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2016· Baxter Healthcare Corp.

Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...

The Issue: Instructions for use booklet may puncture the outer Tyvek lid.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2016· Baxter Healthcare Corp.

Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...

The Issue: Instructions for use booklet may puncture the outer Tyvek lid.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2016· Baxter Healthcare Corp.

Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...

The Issue: Instructions for use booklet may puncture the outer Tyvek lid.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2016· Baxter Healthcare Corp.

Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...

The Issue: Instructions for use booklet may puncture the outer Tyvek lid.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2016· Draeger Medical, Inc.

Recalled Item: Draeger D-Vapor/ D-Vapor 3000 Vaporizers with Baxter Desflurane Agent and...

The Issue: Operators noticed unwanted release of evaporating anesthetic agent at the...

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

Class II — Potential Health HazardOngoing
FoodApril 21, 2016· Vitalicious Acquisition

Recalled Item: VitaTops Apple Crumb Recalled by Vitalicious Acquisition Due to Undeclared Milk

The Issue: The affected lots of VitaTops Apple Crumb contain undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 20, 2016· Harris Teeter

Recalled Item: Gourmet White Chocolate Macadamia Cookies Recalled by Harris Teeter Due to...

The Issue: Undeclared allergen; Peanut Protein

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 20, 2016· Harris Teeter

Recalled Item: Gourmet Cranberry Crunch Cookies Recalled by Harris Teeter Due to Undeclared...

The Issue: Undeclared allergen; Peanut Protein

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 20, 2016· Harris Teeter

Recalled Item: 12 Count Sugar Cookies Recalled by Harris Teeter Due to Undeclared Allergen

The Issue: Undeclared allergen; Peanut Protein

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 20, 2016· Harris Teeter

Recalled Item: Gourmet Oatmeal Raisin Walnut Cookies Recalled by Harris Teeter Due to...

The Issue: Undeclared allergen; Peanut Protein

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 20, 2016· Harris Teeter

Recalled Item: 12 Inch Message Cookies Recalled by Harris Teeter Due to Undeclared Allergen

The Issue: Undeclared allergen; Peanut Protein

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 20, 2016· Acorn Stairlifts, Inc

Recalled Item: Acorn 130 Stairlift Recalled by Acorn Stairlifts, Inc Due to The design of...

The Issue: The design of the seats did not consistently have the adequate strength...

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

Class II — Potential Health HazardOngoing
DrugApril 20, 2016· Pharmakon Pharmaceuticals, Inc.

Recalled Item: Ropivacaine HCI 0.2% in 0.9% Sodium Chloride Recalled by Pharmakon...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund