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. 2,610 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,610 in last 12 months

Showing 1076110780 of 47,654 recalls

Medical DeviceNovember 10, 2022· GE Medical Systems, LLC

Recalled Item: Vivid q ultrasound. Used in ultrasound imaging and analysis in Recalled by...

The Issue: Potential for batteries that have not been replaced at 2 years, as...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2022· GE Medical Systems, LLC

Recalled Item: Vivid q N ultrasound. Not marketed in the US. Used Recalled by GE Medical...

The Issue: Potential for batteries that have not been replaced at 2 years, as...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2022· NuVasive Inc

Recalled Item: X-CORE 2 Ti Core Recalled by NuVasive Inc Due to Potential that insert will...

The Issue: Potential that insert will be unable to disengage from the vertebral body...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2022· GE Medical Systems, LLC

Recalled Item: Vivid S6 N ultrasound. Not marketed in the US. Used Recalled by GE Medical...

The Issue: Potential for batteries that have not been replaced at 2 years, as...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2022· GE Medical Systems, LLC

Recalled Item: Vivid i N ultrasound. Not marketed in the US. Used Recalled by GE Medical...

The Issue: Potential for batteries that have not been replaced at 2 years, as...

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

Class II — Potential Health HazardOngoing
DrugNovember 9, 2022· Lannett Company Inc.

Recalled Item: Triamterene and Hydrochlorothiazide Capsules Recalled by Lannett Company...

The Issue: Failed Impurity/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugNovember 9, 2022· Lannett Company Inc.

Recalled Item: Triamterene and Hydrochlorothiazide Capsules Recalled by Lannett Company...

The Issue: Failed Impurity/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugNovember 9, 2022· ImprimisRx NJ

Recalled Item: Timolol-Latanoprost (0.5/0.005%) ophthalmic drops Recalled by ImprimisRx NJ...

The Issue: Subpotent Drug: The batches contain less than 90% of the labeled amount of...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 9, 2022· ICU Medical Inc

Recalled Item: 0.9% Sodium Chloride Injection Recalled by ICU Medical Inc Due to Lack of...

The Issue: Lack of assurance of sterility: Bags have the potential to leak in the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: ETEST CLINICAL AMIKACIN AK 256 US S30 Recalled by Biomerieux Inc Due to As...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: VITEK 2 REAGENT AST-GN80 TEST KIT 20 CARDS Recalled by Biomerieux Inc Due to...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: PPM LOMBARD PRODUCTS TSA 10PLT Recalled by Biomerieux Inc Due to As the...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: VIDAS CLINICAL VIDAS LISTERIA 60T Recalled by Biomerieux Inc Due to As the...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: VIDAS CLINICAL VIDAS HCG 60 TESTS Recalled by Biomerieux Inc Due to As the...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: PPM INDUSTRY COMBOURG CHROMID CARBA US 20 PLT Recalled by Biomerieux Inc Due...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: ETEST CLINICAL RIFAMPICIN RI 32 US S30 Recalled by Biomerieux Inc Due to As...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: VITEK 2 REAGENT AST-N801 TEST KIT 20 CARDS Recalled by Biomerieux Inc Due to...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: BIOBALL B.SPIZIZENII NCTC 10400 550X20 Recalled by Biomerieux Inc Due to As...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: ETEST CLINICAL MEROPENEM MP 32 US S30 Recalled by Biomerieux Inc Due to As...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: ETEST CLINICAL ERAVACYCLINE ERV US S30 Recalled by Biomerieux Inc Due to As...

The Issue: As the temperature and time out of range was exceeded, product performances...

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

Class II — Potential Health HazardOngoing