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. 2,656 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,656 in last 12 months

Showing 621640 of 47,654 recalls

Medical DeviceNovember 22, 2025· Changchun Wancheng Bio-Electron Co., Ltd.

Recalled Item: LotFancy Urinary Tract Infection Urine (UTI) Test Strips Recalled by...

The Issue: Test strips and other tests including for near-patient testing, that require...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2025· Changchun Wancheng Bio-Electron Co., Ltd.

Recalled Item: Vivoo Vaginal pH Test Recalled by Changchun Wancheng Bio-Electron Co., Ltd....

The Issue: Test strips and other tests including for near-patient testing, that require...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2025· Changchun Wancheng Bio-Electron Co., Ltd.

Recalled Item: The Girlfriend Doctor Dr. Anna Cabeca Keto-pH-Uric Acid Test Strips Recalled...

The Issue: Test strips and other tests including for near-patient testing, that require...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2025· Changchun Wancheng Bio-Electron Co., Ltd.

Recalled Item: Vivoo pH Test Recalled by Changchun Wancheng Bio-Electron Co., Ltd. Due to...

The Issue: Test strips and other tests including for near-patient testing, that require...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2025· Changchun Wancheng Bio-Electron Co., Ltd.

Recalled Item: Vivoo Sodium Test Recalled by Changchun Wancheng Bio-Electron Co., Ltd. Due...

The Issue: Test strips and other tests including for near-patient testing, that require...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2025· Changchun Wancheng Bio-Electron Co., Ltd.

Recalled Item: LH One Step Ovulation Test Device (Urine) Recalled by Changchun Wancheng...

The Issue: Test strips and other tests including for near-patient testing, that require...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2025· Changchun Wancheng Bio-Electron Co., Ltd.

Recalled Item: Menopause Test Cassette (Urine) Recalled by Changchun Wancheng Bio-Electron...

The Issue: Test strips and other tests including for near-patient testing, that require...

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

Class II — Potential Health HazardOngoing
FoodNovember 21, 2025· Silvestri Sweets Inc dba Carousel Candies

Recalled Item: Choceur Pecan Cranberry & Cinnamon Holiday Bark. Standup Pouch Bag. Recalled...

The Issue: Undeclared wheat

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 21, 2025· Silvestri Sweets Inc dba Carousel Candies

Recalled Item: Choceur Cookie Butter Holiday Bark. Standup Pouch Bag. 5 oz. Recalled by...

The Issue: Undeclared pecan

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 21, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Bisoprolol Fumarate and Hydrochlorothiazide Tablets Recalled by Glenmark...

The Issue: Cross Contamination with Other Products: Testing of reserve samples showed...

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 21, 2025· Fresenius Kabi USA, LLC

Recalled Item: Ivenix Infusion System (IIS) Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Emphasizing instructions for LVP duration programming located in the IFU.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2025· Medline Industries, LP

Recalled Item: Medline Hudson RCI Medium Concentration Oxygen Masks: 1041CE MASK Recalled...

The Issue: Firm received multiple complaints regarding tubing disconnecting from oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2025· Roche Diagnostics Operations, Inc.

Recalled Item: The Elecsys Anti-TSHR immunoassay is a three-step competitive immunoassay...

The Issue: Issues identified: 1) Results vary by Instrument Platform; 2) Calibrator...

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

Class II — Potential Health HazardOngoing
DrugNovember 20, 2025· Fagron Compounding Services

Recalled Item: Tropicamide 1%/Cyclopentolate 1%/Phenylephrine 2.5%/Ketorolac 0.5% Topical...

The Issue: Incorrect Product Formulation

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 20, 2025· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedStation ES Recalled by CareFusion 303, Inc. Due to Automated...

The Issue: Automated Dispensing Cabinets (ADC) received a Half Height CUBIE drawer...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2025· Medtronic Neuromodulation

Recalled Item: Restore Clinician Programmer Application (CP App) Recalled by Medtronic...

The Issue: Software issue where a Device Reset message displayed on the app was unable...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2025· Steris Corporation

Recalled Item: AMSCO 7052HP Washer/Disinfector Model/Catalog Number: 7052HP Product...

The Issue: Wire connected to the electrical box may shift out of its intended position,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2025· Steris Corporation

Recalled Item: AMSCO 7053HP Washer/Disinfector Model/Catalog Number: 7053HP Product...

The Issue: Wire connected to the electrical box may shift out of its intended position,...

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

Class II — Potential Health HazardOngoing
DrugNovember 18, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Nebivolol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: Cross Contamination with Other Products

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 18, 2025· AGFA Healthcare Corp.

Recalled Item: Brand name: AGFA Digital Radiography X- Ray system DR 800 Recalled by AGFA...

The Issue: It is possible to exceed the maximum allowed Air Kerma rate (AKR) of...

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

Class II — Potential Health HazardOngoing