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. 1,082 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
1,082 in last 12 months

Showing 1821–1840 of 47,654 recalls

FoodJuly 11, 2025· DANONE US LLC

Recalled Item: YoCrunch Lowfat Yogurt with Toppers Recalled by DANONE US LLC Due to Foreign...

The Issue: Foreign material (plastic pieces)

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 11, 2025· DANONE US LLC

Recalled Item: YoCrunch Low Fat Yogurt with Toppers Recalled by DANONE US LLC Due to...

The Issue: Foreign material (plastic pieces)

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 11, 2025· Flexicare Medical (Dongguan) Ltd.

Recalled Item: BritePro Solo Single-Use Fiber Optic Handle and Blade : 040-331U (Mac 1)...

The Issue: Laryngoscope handles may not illuminate as intended.

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2025· Flexicare Medical (Dongguan) Ltd.

Recalled Item: BritePro Solo Mini Single-Use Fiber Optic Laryngoscope Handle Recalled by...

The Issue: Laryngoscope handles may not illuminate as intended.

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 10, 2025· mo-Vis BVBA

Recalled Item: IDM-ARLITE-R. Electrical wheelchair component. Recalled by mo-Vis BVBA Due...

The Issue: Devices with firmware versions 2.3 and lower may experience timing...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 10, 2025· Biofire Defense

Recalled Item: FilmArray NGDS Warrior Panel NGDS-ASY-0007 is a qualitative Recalled by...

The Issue: FilmArray NGDS Warrior Panel (NGDS-ASY-0007) has an increased risk of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2025· mo-Vis BVBA

Recalled Item: IDM-MULTI-R. Electrical wheelchair component. Recalled by mo-Vis BVBA Due to...

The Issue: Devices with firmware versions 2.3 and lower may experience timing...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 10, 2025· mo-Vis BVBA

Recalled Item: All-round Joystick R-net Light. Electrical wheelchair component. Recalled by...

The Issue: Devices with firmware versions 2.3 and lower may experience timing...

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

Class I — Serious Health HazardOngoing
DrugJuly 10, 2025· A.P. Deauville, LLC

Recalled Item: Shave and Skincare Power Stick Original Nourishing Invisible Protection...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 10, 2025· A.P. Deauville, LLC

Recalled Item: Beauty & Skincare Power Stick original nourishing invisible protection...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 10, 2025· A.P. Deauville, LLC

Recalled Item: Power Stick for her PH Balanced Roll-On Antiperspirant Deodorant with...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 10, 2025· Pfizer Inc.

Recalled Item: Bicillin L-A (penicillin G benzathine injectable suspension) Recalled by...

The Issue: CGMP Deviations; particulates identified during visual inspection

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 10, 2025· Beckman Coulter, Inc.

Recalled Item: Access Thyroglobulin assay Recalled by Beckman Coulter, Inc. Due to Access...

The Issue: Access Thyroglobulin reagent lot 439163 may generate erroneously high...

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

Class II — Potential Health HazardOngoing
DrugJuly 10, 2025· Pfizer Inc.

Recalled Item: Bicillin L-A (penicllin G benzathine injectable suspension) Recalled by...

The Issue: CGMP Deviations; particulates identified during visual inspection

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 10, 2025· mo-Vis BVBA

Recalled Item: IDM-MICRO-R. Electrical wheelchair component. Recalled by mo-Vis BVBA Due to...

The Issue: Devices with firmware versions 2.3 and lower may experience timing...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 10, 2025· mo-Vis BVBA

Recalled Item: Multi Joystick R-net. Electrical wheelchair component. Recalled by mo-Vis...

The Issue: Devices with firmware versions 2.3 and lower may experience timing...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 10, 2025· CareFusion 303, Inc.

Recalled Item: Description/ PYXIS MEDBANK MINI 1FH-1FM/169-137 Recalled by CareFusion 303,...

The Issue: Reports of delayed access to medication in automated dispensing cabinets...

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

Class III — Low RiskOngoing
Medical DeviceJuly 10, 2025· mo-Vis BVBA

Recalled Item: Micro Joystick R-net. Electrical wheelchair component. Recalled by mo-Vis...

The Issue: Devices with firmware versions 2.3 and lower may experience timing...

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

Class I — Serious Health HazardOngoing
DrugJuly 9, 2025· Ascend Laboratories, LLC

Recalled Item: Rizatriptan Benzoate Tablets Recalled by Ascend Laboratories, LLC Due to...

The Issue: CGMP Deviations: detection of N-nitroso-dimethyl-rizatriptan impurity, above...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 9, 2025· Ascend Laboratories, LLC

Recalled Item: Rizatriptan Benzoate Tablets Recalled by Ascend Laboratories, LLC Due to...

The Issue: CGMP Deviations: detection of N-nitroso-dimethyl-rizatriptan impurity, above...

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

Class II — Potential Health HazardOngoing
Refund