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. 2,429 recalls have been distributed to District of Columbia in the last 12 months.
Showing 35741–35760 of 47,654 recalls
Recalled Item: Alaris Syringe Pump Recalled by CareFusion 303, Inc. Due to Channel Error...
The Issue: Channel Error code is displayed on the PC unit with an audio and visual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CrossCHECK Non-Locking Screw in the following sizes: 3.0 x 8 mm Recalled by...
The Issue: These screws have a potential of passing through the plate in the case when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CrossCHECK Locking Screw in the following sizes: 3.0 x 8 mm Recalled by...
The Issue: These screws have a potential of passing through the plate in the case when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phentermine Hydrochloride Capsules Recalled by PD-Rx Pharmaceuticals, Inc....
The Issue: Failed impurities/Degradation specifications: out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Verapamil Hydrochloride Extended-Release tablets Recalled by Apotex Inc. Due...
The Issue: Failed Dissolution Specification: One lot of product did not meet the first...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Concave Reamer Head Recalled by Trilliant Surgical Ltd. Due to The...
The Issue: The cannulation of the Concave and Convex Reamer Heads may be too small to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tiger Cannulated Tray Lid Part # 210-00-001-1 NON-STERILE Recalled by...
The Issue: Sterilization tray lids for the Tiger and Tiger Headless Cannulated Screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.0/4.0 Cannulated Drill Bit Recalled by Trilliant Surgical Ltd. Due to The...
The Issue: The cannulation of the 3.0/4.0 Cannulated Drill Bit inner diamter is too...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune 2 Waste Management System Docking Station (120V and 230V) Recalled...
The Issue: The Fluid Coupling Sleeve, a component within the Neptune Waste Management...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.0/2.4 Cannulated Screw Countersink Part # 210-24-002 NON-STERILE and...
The Issue: The cutting efficiency of the Countersinks was out of specification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ALLOPURINOL TABLETS Recalled by Qualitest Pharmaceuticals Due to Failed...
The Issue: Failed Tablet/Capsule Specifications; report of oversized and discolored tablets
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: buPROPion Hydrochloride Extended-¿release Tablets USP (SR) Recalled by Sun...
The Issue: Failed Dissolution Specification: During analysis of the 18 month long term...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Baxter Healthcare Corp. Due...
The Issue: Presence of Particulate Matter: Customer complaint for an insect found free...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection USP MINI-BAG Plus Container Recalled by...
The Issue: Presence of Particulate Matter: Customer complaint for an insect found free...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LYFO Disk Recalled by Microbiologics Inc Due to LYFO Disk Catalog #0983L is...
The Issue: LYFO Disk Catalog #0983L is to contain Candida tropicalis. However, lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PET Discovery LS Recalled by GE Healthcare Due to Potential for expulsion of...
The Issue: Potential for expulsion of the Power Supply on Lightspeed CT scanner or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wall Chart for STERRAD 100NX System Recalled by Advanced Sterilization...
The Issue: Advanced Sterilization PRoducts (ASP) is recalling the Wall Chart for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lightspeed 16 CT Recalled by GE Healthcare Due to Potential for expulsion of...
The Issue: Potential for expulsion of the Power Supply on Lightspeed CT scanner or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Passive Biopsy Needle Kit Recalled by Medtronic Navigation, Inc....
The Issue: The adhesive between the sphere assembly and the biopsy needle shaft may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PET Discovery ST 16 Recalled by GE Healthcare Due to Potential for expulsion...
The Issue: Potential for expulsion of the Power Supply on Lightspeed CT scanner or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.