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. 2,448 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,448 in last 12 months

Showing 3112131140 of 47,654 recalls

DrugSeptember 20, 2016· Leiter's Compounding

Recalled Item: Vancomycin 10 mg/mL in 0.9% Sodium Chloride (Injection) 1 mL Recalled by...

The Issue: Lack of Assurance of Sterility; all compounded products within expiry...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 20, 2016· Leiter's Compounding

Recalled Item: Cyclopentolate HCl 1% - Tropicamide 1% - PHENYLephrine HCl 2.5% Recalled by...

The Issue: Lack of Assurance of Sterility; all compounded products within expiry...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 20, 2016· Leiter's Compounding

Recalled Item: Placebo for Prednisolone Acetate 1% Recalled by Leiter's Compounding Due to...

The Issue: Lack of Assurance of Sterility; all compounded products within expiry...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 20, 2016· Leiter's Compounding

Recalled Item: Brilliant Blue G 0.025% in 0.9% Sodium Chloride (Injection) 1 Recalled by...

The Issue: Lack of Assurance of Sterility; all compounded products within expiry...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 20, 2016· Leiter's Compounding

Recalled Item: Atropine Sulfate 0.01% in 0.9% Sodium Chloride (Ophthalmic Solution) 10...

The Issue: Lack of Assurance of Sterility; all compounded products within expiry...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 20, 2016· Leiter's Compounding

Recalled Item: Lidocaine HCl 1% - Phenylephrine HCl 1.5% in Sterile Water Recalled by...

The Issue: Lack of Assurance of Sterility; all compounded products within expiry...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 19, 2016· Bausch & Lomb Inc Irb

Recalled Item: PeroxiClear Peroxide Solution Recalled by Bausch & Lomb Inc Irb Due to...

The Issue: Product was found to contain excess residual levels of hydrogen peroxide.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2016· Encore Medical, Lp

Recalled Item: Empowr PS Knee System Box Cut Guide The EMPOWER PS Recalled by Encore...

The Issue: It has been discovered that during Empowr PS Total Knee replacement, while...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2016· Stryker Sustainability Solutions

Recalled Item: Reprocessed Pressure Tourniquet Cuff (PTC) Tourniquet cuffs are single- or...

The Issue: Issue with the process for detection of leaking Pressure Tourniquet Cuffs...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2016· Philips Electronics North America Corporation

Recalled Item: Philips IntelliVue MX40 Patient Monitor: IntelliVue MX40 802.11a/b/g Product...

The Issue: Philips IntelliVue MX40 Patient Wearable Monitor Configuration Setting...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2016· Philips Electronics North America Corporation

Recalled Item: Philips IntelliVue MX40 Patient Monitor: IntelliVue MX40 WMTS Smart-hopping...

The Issue: Philips IntelliVue MX40 Patient Wearable Monitor Configuration Setting...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2016· Philips Electronics North America Corporation

Recalled Item: Philips IntelliVue MX40 Patient Monitor: IntelliVue MX40 Smart-hopping...

The Issue: Philips IntelliVue MX40 Patient Wearable Monitor Configuration Setting...

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

Class II — Potential Health HazardOngoing
FoodSeptember 17, 2016· Mccormick

Recalled Item: Club Size McCormick Original Taco Seasoning Mix 24 oz. Recalled by Mccormick...

The Issue: Product was recalled due to undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 16, 2016· National Foods Packaging Inc

Recalled Item: Hillcrest Farms Poultry Gravy Mix in 25lb brown poly-lined bags Recalled by...

The Issue: Product contains a spice which was tested and found to contain elevated...

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

Class III — Low RiskOngoing
Refund
FoodSeptember 16, 2016· National Foods Packaging Inc

Recalled Item: National Foods Packaging Chicken Base in 25 lb white poly-lined paper bags...

The Issue: Product contains a spice which was tested and found to contain elevated...

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

Class III — Low RiskOngoing
Refund
FoodSeptember 16, 2016· National Foods Packaging Inc

Recalled Item: National Foods Packaging Low Sodium Chicken Base in 50 lb Recalled by...

The Issue: Product contains a spice which was tested and found to contain elevated...

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 16, 2016· Becton Dickinson & Company

Recalled Item: BD SafetyGlide" Injection Needle Catalog #305917 The SafetyGlide " needle...

The Issue: BD identified that several lots did not receive the specified dose of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2016· Vascular Solutions, Inc.

Recalled Item: Vascular Solutions Twin-Pass Dual Access Catheter Recalled by Vascular...

The Issue: Vascular Solutions is recalling Twin-Pass dual access catheters because...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 16, 2016· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: RTI Surgical Streamline OCT Occipito-Cervico-Thoracic Spinal Rod Recalled by...

The Issue: RTI Surgical Inc. (RTI) is conducting a voluntary recall on two specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2016· Vascular Solutions, Inc.

Recalled Item: Vascular Solutions Twin-Pass RX Dual Access Catheter Recalled by Vascular...

The Issue: Vascular Solutions is recalling Twin-Pass dual access catheters because...

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

Class I — Serious Health HazardOngoing