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. 2,373 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,373 in last 12 months

Showing 4404144060 of 47,654 recalls

Medical DeviceMay 10, 2013· Symbios Medical Products, LLC

Recalled Item: Part510447 Disposable Infusion Pump Recalled by Symbios Medical Products,...

The Issue: Symbios Medical Products, Indianapolis, Indiana, is performing a voluntary...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2013· Symbios Medical Products, LLC

Recalled Item: Part 510450 Disposable Infusion Pump Recalled by Symbios Medical Products,...

The Issue: Symbios Medical Products, Indianapolis, Indiana, is performing a voluntary...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2013· Symbios Medical Products, LLC

Recalled Item: Part 510076 Disposable Dual Infusion Pump Recalled by Symbios Medical...

The Issue: Symbios Medical Products, Indianapolis, Indiana, is performing a voluntary...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2013· Symbios Medical Products, LLC

Recalled Item: Part 510121 Disposable Infusion Pump Recalled by Symbios Medical Products,...

The Issue: Symbios Medical Products, Indianapolis, Indiana, is performing a voluntary...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2013· Symbios Medical Products, LLC

Recalled Item: Part 510613 Disposable Infusion Pump Recalled by Symbios Medical Products,...

The Issue: Symbios Medical Products, Indianapolis, Indiana, is performing a voluntary...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2013· Symbios Medical Products, LLC

Recalled Item: Part 510613 Disposable Infusion Pump Recalled by Symbios Medical Products,...

The Issue: Symbios Medical Products, Indianapolis, Indiana, is performing a voluntary...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2013· Symbios Medical Products, LLC

Recalled Item: Part 510031 Disposable Single Infusion Pump Recalled by Symbios Medical...

The Issue: Symbios Medical Products, Indianapolis, Indiana, is performing a voluntary...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 9, 2013· Novarad Corporation

Recalled Item: NovaPACS  versions 7.4 Recalled by Novarad Corporation Due to Potential for...

The Issue: Potential for images to be flipped while streaming, which could incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2013· Integra LifeSciences Corporation

Recalled Item: Integra PANTA Arthrodesis Nail System. Intended for use in...

The Issue: As a result of the investigation into an adverse trend of complaints for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products CRP Slides (Reagent) Recalled by Ortho-Clinical...

The Issue: While performing interval testing Ortho Clinical Diagnostics (OCD)...

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

Class III — Low RiskOngoing
Medical DeviceMay 9, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products K+ (Potassium) Slides (Reagent) Recalled by...

The Issue: While performing interval testing, Ortho Clinical Diagnostics (OCD)...

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

Class III — Low RiskOngoing
Medical DeviceMay 9, 2013· ConBio, a CynoSure Company

Recalled Item: Multilite Dye Handpieces Recalled by ConBio, a CynoSure Company Due to An...

The Issue: An inconsistency was identified related to electronic display identification...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2013· Verathon, Inc.

Recalled Item: GlideScope Video Laryngoscope (GVL) 3 Recalled by Verathon, Inc. Due to...

The Issue: Verathon GlideScope Reusable GVL and AVL Blades are being recalled due to...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 8, 2013· Intuitive Surgical, Inc.

Recalled Item: 8 mm Monopolar Curved Scissors (a.k.a. Hot Shears) Manufactured and Recalled...

The Issue: Intuitive Surgical has identified a potential for some units of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2013· Intuitive Surgical, Inc.

Recalled Item: 8mm Maryland Bipolar Forceps used in conjunction with the da Recalled by...

The Issue: Reports of dislodging of the Cautery Plug Insert from the Cautery Plug...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2013· Intuitive Surgical, Inc.

Recalled Item: 8mm Precise Bipolar Forceps used in conjunction with the da Recalled by...

The Issue: Reports of dislodging of the Cautery Plug Insert from the Cautery Plug...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2013· Intuitive Surgical, Inc.

Recalled Item: 8mm Fenestrated Bipolar Forceps used in conjunction with the da Recalled by...

The Issue: Reports of dislodging of the Cautery Plug Insert from the Cautery Plug...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2013· DePuy Orthopaedics, Inc.

Recalled Item: DePuy LifeLiner Stick & Cut Resistant Gloves Rt Recalled by DePuy...

The Issue: LifeLiner Stick and Cut Resistant Gloves are being recalled because cases...

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

Class III — Low RiskOngoing
DrugMay 7, 2013· Hill Dermaceuticals, Inc.

Recalled Item: Derma-Smoothe/FS (fluocinolone acetonide) Topical Oil (SCALP OIL) Recalled...

The Issue: Subpotent Drug: the active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
FoodMay 7, 2013· Novartis Consumer Health

Recalled Item: Benefiber Fiber Drink Mix Recalled by Novartis Consumer Health Due to The...

The Issue: The products are being recalled due to the receipt of a relatively high...

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

Class II — Potential Health HazardOngoing
Refund