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. 2,542 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,542 in last 12 months

Showing 1860118620 of 47,654 recalls

Medical DeviceMarch 30, 2020· Beckman Coulter Inc.

Recalled Item: iQ200 Series Urine Microscopy Analyzer- All part numbers Recalled by Beckman...

The Issue: A defect in the SATA power adapter cable within the instrument s computer...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2020· Boston Scientific Corporation

Recalled Item: MoXy Laser Fiber Recalled by Boston Scientific Corporation Due to To...

The Issue: To reinforce existing instructions within the Directions for Use (DFU) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2020· Elekta Inc

Recalled Item: Leksell Vantage Stereotactic System. Instrument Carrier Recalled by Elekta...

The Issue: A faulty locking piece of the Instrument Carrier that does not fulfil the...

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

Class II — Potential Health HazardOngoing
DrugMarch 26, 2020· Avet Pharmaceuticals, Inc.

Recalled Item: Losartan Potassium Tablets USP 100 mg Recalled by Avet Pharmaceuticals, Inc....

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 26, 2020· Avet Pharmaceuticals, Inc.

Recalled Item: Losartan Potassium Tablets USP 50 mg Recalled by Avet Pharmaceuticals, Inc....

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 26, 2020· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: Positron Emission Tomography and Computed Tomography System Recalled by...

The Issue: In affected software version, of Positron emission tomography and computed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2020· Medtronic Sofamor Danek USA Inc

Recalled Item: VERTEX SELECT MULTI AXIAL SCREW. 4.0 X 38MM MULTI AXIAL SCREW. Lot H5517628...

The Issue: Nonconforming product; length of the product measured shorter than the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2020· Gentell, Inc

Recalled Item: Gentell Honey Hydrogel 2"x2" Saturated Gauze- A hydrating wound dressing...

The Issue: During an FDA audit, it was discovered that the product was not properly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2020· Gentell, Inc

Recalled Item: Gentell Honey Hydrogel 4"x8" Saturated Gauze- A hydrating wound dressing...

The Issue: During an FDA audit, it was discovered that the product was not properly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2020· Gentell, Inc

Recalled Item: Gentell Honey Hydrogel Hydrogel 4oz. Tube. Wound dressing containing...

The Issue: During an FDA audit, it was discovered that the product was not properly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2020· Gentell, Inc

Recalled Item: Gentell Honey Hydrogel 4"x4" Saturated Gauze- A hydrating wound dressing...

The Issue: During an FDA audit, it was discovered that the product was not properly...

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

Class II — Potential Health HazardOngoing
DrugMarch 25, 2020· Akorn Inc

Recalled Item: Fentanyl Citrate Injection Recalled by Akorn Inc Due to Failed...

The Issue: Failed impurities/degradation specification: Out-of-Specification result for...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 25, 2020· Abbott Vascular

Recalled Item: Xience Sierra TM Everolimus Eluting Coronary Stent System Recalled by Abbott...

The Issue: Incorrect expiration date

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

Class II — Potential Health HazardOngoing
DrugMarch 23, 2020· Avet Pharmaceuticals, Inc.

Recalled Item: Tetracycline HCL Capsules Recalled by Avet Pharmaceuticals, Inc. Due to...

The Issue: Failed Dissolution Specifications: Out of specification result during long...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 23, 2020· Avet Pharmaceuticals, Inc.

Recalled Item: Tetracycline HCL Capsules Recalled by Avet Pharmaceuticals, Inc. Due to...

The Issue: Failed Dissolution Specifications: Out of specification result during long...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 23, 2020· Mylan Pharmaceuticals Inc.

Recalled Item: Tacrolimus Capsules Recalled by Mylan Pharmaceuticals Inc. Due to Presence...

The Issue: Presence of foreign tablet/capsule - Potential presence of commingled one...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 23, 2020· INARI MEDICAL

Recalled Item: Triever20 Aspiration Guide Catheter a component of FlowTriever Retrieval/...

The Issue: The hemostasis valve of aspiration guide catheter devices may fail to seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2020· The Magstim Company Limited

Recalled Item: Horizon PSU Stim Interconnecting Cable - Product Usage: Horizon is Recalled...

The Issue: It was identified that there is a potential for the Stim Interconnecting...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2020· The Magstim Company Limited

Recalled Item: Rapid2 PSU Stim Interconnecting Cable - Product Usage: indicated for...

The Issue: It was identified that there is a potential for the Stim Interconnecting...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Pleuravideoscope Recalled by Olympus Corporation of the Americas Due...

The Issue: There was no data to validate that the identified endo-therapy devices were...

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

Class II — Potential Health HazardOngoing