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. 2,395 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,395 in last 12 months

Showing 441460 of 47,654 recalls

DrugDecember 16, 2025· SpecGx, LLC

Recalled Item: Oxycodone and Acetaminophen CII Tablets USP Recalled by SpecGx, LLC Due to...

The Issue: Failed Tablet/Capsule Specification: There is a potential for the imprint to...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Vortex Surgical 25GA I.D.D. Internal Delivery Device Recalled by Vortex...

The Issue: There may be voids located in the seal of Tyvek pouches associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: 25GA Subretinal Injection Cannula VS0220.25 Recalled by Vortex Surgical Inc....

The Issue: There may be voids located in the seal of Tyvek pouches associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Tecfen Retractable Membrane Polisher Recalled by Vortex Surgical Inc. Due to...

The Issue: There may be voids located in the seal of Tyvek pouches associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) THORACIC ROBOTICS...

The Issue: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Vortex Surgical 25GA Backflush Recalled by Vortex Surgical Inc. Due to There...

The Issue: There may be voids located in the seal of Tyvek pouches associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) LAVH PROCEDURE...

The Issue: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Volk Single Use Vitrectomy Lenses 1. Flat Vitrectomy Lens Recalled by Vortex...

The Issue: There may be voids located in the seal of Tyvek pouches associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Rumex Disposable Diamond Dusted ILM Elevator Recalled by Vortex Surgical...

The Issue: There may be voids located in the seal of Tyvek pouches associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Vortex Disposable Forceps and Cannula 1. 23GA ACTU8 Forceps Adaptive...

The Issue: There may be voids located in the seal of Tyvek pouches associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Vortex Surgical Lindsell Sutured IOL Marker Recalled by Vortex Surgical Inc....

The Issue: There may be voids located in the seal of Tyvek pouches associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: KIT ROBOTICS UROLOGY...

The Issue: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) LAPAROSCOPY CDS-LF...

The Issue: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) WCH...

The Issue: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a...

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

Class II — Potential Health HazardOngoing
DrugDecember 15, 2025· NOVADOZ PHARMACEUTICALS LLC

Recalled Item: Glycopyrrolate Oral Solution Recalled by NOVADOZ PHARMACEUTICALS LLC Due to...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 15, 2025· SunMed Holdings, LLC

Recalled Item: Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape...

The Issue: Product contains potentially harmful dosing errors for Vecuronium,...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 15, 2025· SunMed Holdings, LLC

Recalled Item: Brand Name: Broselow Product Name: Broselow Domestic Complete ALS Organizer...

The Issue: Product contains potentially harmful dosing errors for Vecuronium,...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 15, 2025· Hologic, Inc

Recalled Item: Brevera Breast Biopsy System Disposable 9 Gauge Needle. Biopsy Instrument....

The Issue: Presence of particulates in affected devices that can be deposited into...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· SunMed Holdings, LLC

Recalled Item: Brand Name: Broselow Product Name: BROSELOW" FILLED BROSELOW ORGANIZER...

The Issue: Product contains potentially harmful dosing errors for Vecuronium,...

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

Class I — Serious Health HazardOngoing
FoodDecember 15, 2025· WhiteWave - Louisville Pilot Plant

Recalled Item: So Delicious Dairy Free Salted Caramel Cluster Cashewmilk Recalled by...

The Issue: Foreign material

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

Class II — Potential Health HazardOngoing
Refund