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. 2,360 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,360 in last 12 months

Showing 4700147020 of 47,654 recalls

Medical DeviceMay 11, 2012· Vygon Corporation

Recalled Item: Vygon VY(TM)Flush Heparin Lock Flush Syringes Recalled by Vygon Corporation...

The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Vygon Corporation

Recalled Item: Churchill Medical Systems Recalled by Vygon Corporation Due to Manufacturer...

The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Vygon Corporation

Recalled Item: Vygon VY(TM)Flush Heparin Lock Flush Syringes Recalled by Vygon Corporation...

The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...

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

Class II — Potential Health HazardOngoing
DrugMay 9, 2012· Grandpa Brands Co

Recalled Item: Dent's Extra Strength Toothache Gum Recalled by Grandpa Brands Co Due to...

The Issue: Superpotent; benzocaine

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 9, 2012· SpineFrontier, Inc.

Recalled Item: Invue Solid Driver Recalled by SpineFrontier, Inc. Due to The nipple of the...

The Issue: The nipple of the tipped driver broke off when surgeons were attempting to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Natus Medical Incorporated

Recalled Item: The product has the Catalogue/Part number 60010. Olympic Cool-Cap System...

The Issue: The Olympic Cool-Cap's Control Module has experienced a frozen screen during...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 9, 2012· RAYSEARCH LABORATORIES AB

Recalled Item: Brand name: RayStation. Generic name: Treatment Planning System. Software...

The Issue: The firm decided to recall when an issue was found with the dose calculation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Antegrade Cardioplegia Cannula: ROOT INFUSTION VENT CATHETER WITH 12...

The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: X-COATED TRANSPLANT PACK Product Usage: The Sarns Cardioplegia Cannula and...

The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: FX PACK Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent...

The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: SARNS ANTEGRADE CARDIOPLEGIA CANNULA: ROOT INFUSION CANNULA WITH 12-GAUGE...

The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: INDIANA/OHIO HEART Product Usage: The Sarns Cardioplegia Cannula and...

The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: CPB CATHETER KIT-DR VANTRIGHT Product Usage: The Sarns Cardioplegia Cannula...

The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: SARNS ANTEGRADE CARDIOPLEGIA CANNULA: ROOT INFUSION CANNULA WITH 14-GAUGE...

The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: X-COATED H/L PK W/FX15RW40 Product Usage: The Sarns Cardioplegia Cannula...

The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: CPB CATHETER KIT- DR HENDRICKSO Product Usage: The Sarns Cardioplegia...

The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: X-COATED SMALL PATIENT PACK Product Usage: The Sarns Cardioplegia Cannula...

The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: X-COATED FX25RW H/L PACK Product Usage: The Sarns Cardioplegia Cannula...

The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: CPB CATHETER KIT- DR OWEN Product Usage: The Sarns Cardioplegia Recalled by...

The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: X-COATED SMALL PATIENT PACK Product Usage: The Sarns Cardioplegia Cannula...

The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...

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

Class II — Potential Health HazardOngoing