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.
Showing 31821–31840 of 47,654 recalls
Recalled Item: Orthopedic manual surgical instrument Usage: Exeter Rasp Handle is a...
The Issue: Malfunctioning of the Exeter Rasp/trial introducer/extractor Handle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra External Fixation System Rocker Bottom Model # 12225400. For...
The Issue: The silicone insert embedded in the rocker bottom has the potential to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TAZORAC (tazarotene) Gel 0.05% Recalled by Allergan Sales, LLC Due to Failed...
The Issue: Failed Content Uniformity Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TAZORAC (tazarotene) Gel 0.05% Recalled by Allergan Sales, LLC Due to Failed...
The Issue: Failed Content Uniformity Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glipizide 2.5 mg Extended-release tablets Recalled by Actavis Inc Due to...
The Issue: Failed Dissolution Specifications: Glipizide 2.5 mg ER Tablets exceeded...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zyston¿ Transform Instrument Case. Model Number PCR8200-2101. Device labeled...
The Issue: Zimmer Bioment Spine, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zyston¿ Transform Implant Kit. Model Number PCR8200-3101. Device labeled...
The Issue: Zimmer Bioment Spine, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avenir M¿ller Stem 4 Standard Avenir M¿ller Stem 6 Lateral Recalled by...
The Issue: Product mix-up. The Avenir M¿ller Stem 6 lateral uncemented might be placed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Methylprednisolone Acetate/Lidocaine HCl 40/10 mg/mL Injection Recalled by...
The Issue: Lack of Processing Controls: Isomeric Pharmacy Solution, LLC announces a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TRYX Antibacterial Envelope Rx Only Product Usage: Indicated for...
The Issue: TRYX products are being recalled since the processes of spaying, welding,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRYX Absorbable Antibacterial Envelope Product Usage: Indicated for...
The Issue: TRYX products are being recalled since the processes of spaying, welding,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRYX Neuro Absorbable Antibacterial Envelope Product Usage: Indicated for...
The Issue: TRYX products are being recalled since the processes of spaying, welding,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureStep Tray Recalled by C.R. Bard, Inc. Due to Labeling problem
The Issue: Labeling problem
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DULOXETINE Delayed-Release Capsules Recalled by Golden State Medical Supply...
The Issue: Labeling; Incorrect or Missing Lot and/or Exp Date; incorrect expiration...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NIM EMG Endotracheal Tube Recalled by Medtronic Xomed, Inc. Due to Wire in...
The Issue: Wire in tubing can become exposed, posing potential harm to the intubated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with Recalled...
The Issue: Product gives incorrect low blood glucose levels.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with Recalled...
The Issue: Product gives incorrect low blood glucose levels.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with Recalled...
The Issue: Product gives incorrect low blood glucose levels.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with Recalled...
The Issue: Product gives incorrect low blood glucose levels.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spirit Plus Bed Recalled by CHG Hospital Beds Inc Due to Stryker Medical is...
The Issue: Stryker Medical is initiating a voluntary recall of the Spirit Select and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.