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. 2,395 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,395 in last 12 months

Showing 4306143080 of 47,654 recalls

Medical DeviceJuly 16, 2013· Assuramed

Recalled Item: Hemoccult II BRAND SENSA elite Recalled by Assuramed Due to The products may...

The Issue: The products may have been stored at temperatures outside their required...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2013· Zimmer, Inc.

Recalled Item: Moore Hip Prosthesis Long Fenestrated Stem Recalled by Zimmer, Inc. Due to...

The Issue: Zimmer recently conducted a review of historic packaging validations...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2013· Atrium Medical Corporation

Recalled Item: PleuraGuide Disposable Chest Tube Kit Recalled by Atrium Medical Corporation...

The Issue: Individual component's IFUs are not included with the kit.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2013· HemoCue AB

Recalled Item: HemoCue¿ Glucose 201 Microcuvettes Recalled by HemoCue AB Due to During a...

The Issue: During a complaint investigation HemoCue AB discovered punctured HemoCue...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2013· DeRoyal Industries Inc

Recalled Item: DeRoyal Insufflation Tubing sets: 1) Insufflation Tubing Recalled by DeRoyal...

The Issue: DeRoyal Industries is recalling their product Insufflation Tubing Sets due...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2013· Nova Biomedical Corporation

Recalled Item: Nova Max Glucose Test Strips (100 Count Retail Canada)Catalog Number:...

The Issue: Reports of false abnormally high glucose readings from test strips

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 15, 2013· Nova Biomedical Corporation

Recalled Item: Nova Max Glucose Test Strips (50 Count International Catalog Number:...

The Issue: Reports of false abnormally high glucose readings from test strips

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 15, 2013· Nova Biomedical Corporation

Recalled Item: Nova Max Glucose Test Strips (10 Count Canada)Catalog Number: 43877 Recalled...

The Issue: Reports of false abnormally high glucose readings from test strips

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 15, 2013· Nova Biomedical Corporation

Recalled Item: Nova Max Plus Monitor System (Kit w/10 Count Vials International) Recalled...

The Issue: Reports of false abnormally high glucose readings from test strips

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 15, 2013· Nova Biomedical Corporation

Recalled Item: Nova Max Glucose Test Strips (10 Count Vials) Catalog Number: Recalled by...

The Issue: Reports of false abnormally high glucose readings from test strips

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 15, 2013· Nova Biomedical Corporation

Recalled Item: Nova Max Plus Monitor System (Kit w/10 Count Vials) Catalog Recalled by Nova...

The Issue: Reports of false abnormally high glucose readings from test strips

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 15, 2013· Nova Biomedical Corporation

Recalled Item: Nova Max Plus Monitor System (Kit w/10 Count Vials Canada) Recalled by Nova...

The Issue: Reports of false abnormally high glucose readings from test strips

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 15, 2013· Nova Biomedical Corporation

Recalled Item: Nova Max Glucose Test Strips (50 Count DME) Catalog Number: Recalled by Nova...

The Issue: Reports of false abnormally high glucose readings from test strips

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 15, 2013· Nova Biomedical Corporation

Recalled Item: Nova Max Glucose Test Strips (10 Count Boxed) Catalog Number: Recalled by...

The Issue: Reports of false abnormally high glucose readings from test strips

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 15, 2013· Nova Biomedical Corporation

Recalled Item: Nova Max Glucose Test Strips (50 Count Retail) Catalog Number: Recalled by...

The Issue: Reports of false abnormally high glucose readings from test strips

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

Class I — Serious Health HazardOngoing
DrugJuly 12, 2013· Hospira Inc.

Recalled Item: 0.25% Bupivacaine HCl Injection Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of particulate matter: visible free floating and partially embedded...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 12, 2013· Hospira Inc.

Recalled Item: 0.75% Bupivacaine HCl Injection Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of particulate matter: visible free floating and partially embedded...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Flixene Grafts >or= 6mm Intended for use in arterial vascular reconstruction...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Advanta VS Grafts >or= 6mm Intended for use in arterial vascular...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Advanta VXT Vascular Grafts >or= 6mm Intended for use in Recalled by Atrium...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing