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. 2,655 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,655 in last 12 months

Showing 24612480 of 47,654 recalls

Medical DeviceMay 1, 2025· Remel, Inc

Recalled Item: Thermo SCIENTIFIC Sensititre Cation Adjusted AutoRead Mueller-Hinton Broth...

The Issue: Product may have an off color affecting perfomance

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2025· SunMed Holdings, LLC

Recalled Item: Adult Manual Resuscitator with Medium Adult Mask Recalled by SunMed...

The Issue: Affected lots were manufactured with B/V Filter incorrectly attached to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 1, 2025· Straumann USA LLC

Recalled Item: GM Helix Acqua Implant Recalled by Straumann USA LLC Due to It is possible...

The Issue: It is possible that a package labelled as an 11.5 mm implant may contain a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2025· Straumann USA LLC

Recalled Item: GM Helix Acqua Implant Recalled by Straumann USA LLC Due to It is possible...

The Issue: It is possible that a package labelled as an 11.5 mm implant may contain a...

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

Class II — Potential Health HazardOngoing
FoodApril 30, 2025· Preventics, Inc. dba Legere Pharmaceuticals

Recalled Item: Rodex Forte Recalled by Preventics, Inc. dba Legere Pharmaceuticals Due to...

The Issue: Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in...

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

Class III — Low RiskOngoing
Refund
FoodApril 30, 2025· Preventics, Inc. dba Legere Pharmaceuticals

Recalled Item: Prothin Recalled by Preventics, Inc. dba Legere Pharmaceuticals Due to...

The Issue: Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in...

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

Class III — Low RiskOngoing
Refund
FoodApril 30, 2025· Preventics, Inc. dba Legere Pharmaceuticals

Recalled Item: Probese Caps Recalled by Preventics, Inc. dba Legere Pharmaceuticals Due to...

The Issue: Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in...

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

Class III — Low RiskOngoing
Refund
FoodApril 30, 2025· Preventics, Inc. dba Legere Pharmaceuticals

Recalled Item: Super ProTHIN Plus Recalled by Preventics, Inc. dba Legere Pharmaceuticals...

The Issue: Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in...

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

Class III — Low RiskOngoing
Refund
FoodApril 30, 2025· Preventics, Inc. dba Legere Pharmaceuticals

Recalled Item: NutriLean Recalled by Preventics, Inc. dba Legere Pharmaceuticals Due to...

The Issue: Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in...

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

Class III — Low RiskOngoing
Refund
FoodApril 30, 2025· Preventics, Inc. dba Legere Pharmaceuticals

Recalled Item: Protrim Plus Recalled by Preventics, Inc. dba Legere Pharmaceuticals Due to...

The Issue: Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in...

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 30, 2025· Beckman Coulter Mishima K.K.

Recalled Item: Sample probe sucks a sample dispensed into a tube or Recalled by Beckman...

The Issue: A manufacturing defect in the sample probe (S probe). The corners of the tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2025· Beckman Coulter Mishima K.K.

Recalled Item: Sample probe sucks a sample dispensed into a tube or Recalled by Beckman...

The Issue: Sample probes with defective probe tips, when used with clinical chemistry...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2025· Fresenius Medical Care Holdings, Inc.

Recalled Item: 5008X HDF Hemodialysis Blood Tubing Set Recalled by Fresenius Medical Care...

The Issue: Potential of blood leak occurring between the lower port of the venous...

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

Class II — Potential Health HazardOngoing
DrugApril 28, 2025· Siddha Flower Essences, LLC.

Recalled Item: temper tamer Recalled by Siddha Flower Essences, LLC. Due to CGMP Deviations

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 28, 2025· BSO LLC

Recalled Item: TESTOSTERONE PELLET 100 mg (with Cholesterol </=4%) Recalled by BSO LLC Due...

The Issue: Presence of Particulate Matter: Glass particles were found in pellet vials.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 28, 2025· BSO LLC

Recalled Item: TESTOSTERONE PELLET 200 mg BLUNT Recalled by BSO LLC Due to Presence of...

The Issue: Presence of Particulate Matter: Glass particles were found in pellet vials.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 28, 2025· BSO LLC

Recalled Item: TESTOSTERONE PELLET 200 mg (with Cholesterol </=4%) Recalled by BSO LLC Due...

The Issue: Presence of Particulate Matter: Glass particles were found in pellet vials.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 28, 2025· BSO LLC

Recalled Item: TESTOSTERONE PELLET 200 mg BLUNT (with Cholesterol </=2%) Recalled by BSO...

The Issue: Presence of Particulate Matter: Glass particles were found in pellet vials.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 28, 2025· BSO LLC

Recalled Item: TESTOSTERONE PELLET 200 mg (with Cholesterol </=2%) Recalled by BSO LLC Due...

The Issue: Presence of Particulate Matter: Glass particles were found in pellet vials.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 28, 2025· Alcon Research LLC

Recalled Item: Brand Name: Alcon Laboratories Recalled by Alcon Research LLC Due to Due to...

The Issue: Due to the potential that some units within specific lots were damaged...

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

Class II — Potential Health HazardOngoing