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. 2,496 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,496 in last 12 months

Showing 2078120800 of 47,654 recalls

Medical DeviceJuly 23, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: Online TDM Vancomycin Gen.3 (100 tests) Catalog # 06779336190...

The Issue: Inaccurately Low Sample Results

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2019· New Standard Device Inc

Recalled Item: 'n'-Hole Post which is a component of the Revolution External Recalled by...

The Issue: The threads on posts stripping out when tensioned during application process.

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

Class II — Potential Health HazardOngoing
DrugJuly 23, 2019· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Mometasone Furoate Cream USP Recalled by Glenmark Pharmaceuticals Inc., USA...

The Issue: GMP Deviations: Glenmark received complaints stating that mometasone fuorate...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 22, 2019· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur Folate (500 Test Kit)-for IVD of folate Recalled by...

The Issue: Homocysteine Assay May Cause Elevated Results in the Folate Assay

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2019· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur Folate 100 test kit-for IVD of folate Recalled by...

The Issue: Homocysteine Assay May Cause Elevated Results in the Folate Assay

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2019· DeRoyal Industries Inc

Recalled Item: DeRoyal Enteral Safe Feeding Tubes: a) Recalled by DeRoyal Industries Inc...

The Issue: Certain MED-RX Polyurethane Feeding Tubes are being recalled due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2019· Zeus Scientific, Inc.

Recalled Item: Dynex DSX Software-IVD ELISA Assays effected as follows: DSX Assay Recalled...

The Issue: Assay files used on the open Dynex DSX Instrument to process IVD ELISA...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2019· GETINGE US SALES LLC

Recalled Item: Getinge MCC Flow i Disposable CO2 absorber Recalled by GETINGE US SALES LLC...

The Issue: Reversed expiration and manufacturing date on the label

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2019· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur Folate (500 Test Kit )- for IVD Recalled by Siemens...

The Issue: Homocysteine Assay May Cause Elevated Results in the Folate Assay

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2019· Philips North America, LLC

Recalled Item: Philips 5-Lead Set Recalled by Philips North America, LLC Due to The...

The Issue: The thickness of the connector to the trunk cable on affected limb lead sets...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2019· Cincinnati Sub-Zero Products LLC, a Gentherm Company

Recalled Item: MICRO-TEMP LT System Recalled by Cincinnati Sub-Zero Products LLC, a...

The Issue: Updated Manual-Warnigs have been added stating that exceeding 40'C for...

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

Class III — Low RiskOngoing
Medical DeviceJuly 19, 2019· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm FDR Go Plus mobile X-ray system Recalled by Fujifilm Medical...

The Issue: The graphics driver of the FDR Go PLUS might cause the appearance of a Blue...

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

Class II — Potential Health HazardOngoing
DrugJuly 19, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Lisinopril and Hydrochlorothiazide Tablets USP Recalled by Lupin...

The Issue: Presence of Foreign Tablets/Capsules: Product complaint received of one...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 19, 2019· Dercher Enterprises, Inc., DBA Gordon Laboratories

Recalled Item: MONSEL'S (Ferric Subsulfate) Solution Recalled by Dercher Enterprises, Inc.,...

The Issue: Microbial Contamination of Non-Sterile Products and Superpotent Drug: FDA...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 18, 2019· Baxter Healthcare Corporation

Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Baxter Healthcare Corporation...

The Issue: Lack of Assurance of Sterility: Bags have potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 18, 2019· Amneal Pharmaceuticals, Inc.

Recalled Item: Methylergonovine Maleate USP 0.2 mg Tablets a) 12 count (NDC Recalled by...

The Issue: Presence of Foreign Tablet/Capsule; one Promethazine tablet was found in a...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 18, 2019· Arrow International Inc

Recalled Item: Arrow AGB+ Multi-Lumen CVC Kit-catheter permits venous access to central...

The Issue: Arrow AGB+ Multi-Lumen CVC Kit - lidstock incorrectly states within...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2019· Medical Intelligence Medizintechnik Gmbh

Recalled Item: IGuide System Recalled by Medical Intelligence Medizintechnik Gmbh Due to...

The Issue: Sometimes, although the HexaPOD has reached the target position, the...

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

Class II — Potential Health HazardOngoing
FoodJuly 18, 2019· Mountain Rose Inc. dba Mountain Rose Herbs

Recalled Item: Fennel Whole Seed was packaged in a clear plastic bag Recalled by Mountain...

The Issue: Fennel Whole Seed is recalled due to a potential for contamination with...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 17, 2019· ImprimisRx NJ

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

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund