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 10411060 of 27,451 recalls

Medical DeviceSeptember 3, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20/15 OR Table Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...

The Issue: Systems may not perform as intended due to the deterioration of certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD10 OR Table Product Codes: (1)722022 Recalled by PHILIPS...

The Issue: Systems may not perform as intended due to the deterioration of certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura CV20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: Systems may not perform as intended due to the deterioration of certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD10 Product Codes: (1)722010 Recalled by PHILIPS MEDICAL...

The Issue: Systems may not perform as intended due to the deterioration of certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20 OR Table Product Codes: (1)722023 Recalled by PHILIPS...

The Issue: Systems may not perform as intended due to the deterioration of certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20/20 OR Table Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...

The Issue: Systems may not perform as intended due to the deterioration of certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20 Biplane OR Table Product Codes: (1)722020 Recalled by...

The Issue: Systems may not perform as intended due to the deterioration of certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20 Product Codes: (1)722012 Recalled by PHILIPS MEDICAL...

The Issue: Systems may not perform as intended due to the deterioration of certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20/20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...

The Issue: Systems may not perform as intended due to the deterioration of certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20/10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...

The Issue: Systems may not perform as intended due to the deterioration of certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2025· Berkeley Advanced Biomaterials, LLC

Recalled Item: Tribio Implant 7.5mm x 40mm SB008 UDI code: Recalled by Berkeley Advanced...

The Issue: Due to incorrect product label (Incorrect product name identified on outer...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2025· LeMaitre Vascular, Inc.

Recalled Item: Artegraft Collagen Vascular Grafts Model Numbers: (1) AG 616 Recalled by...

The Issue: The bovine carotid arteries used to produce the impacted grafts from...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK System Solution Set Recalled by Baxter Healthcare Corporation Due...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK SYSTEM CONTINU-FLO Solution Set Recalled by Baxter Healthcare...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK SYSTEM CONTINU-FLO Solution Set Recalled by Baxter Healthcare...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK SYSTEM EXTENSION SET Recalled by Baxter Healthcare Corporation Due...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK SYSTEM CONTINU-FLO Solution Set Recalled by Baxter Healthcare...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK SYSTEM CONTINU-FLO Solution Set Recalled by Baxter Healthcare...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK SYSTEM NON-DEHP CONTINU-FLO SOLN SET Recalled by Baxter Healthcare...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK System Paclitaxel Set Recalled by Baxter Healthcare Corporation...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing