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. 944 recalls have been distributed to District of Columbia in the last 12 months.
Showing 34041–34060 of 47,654 recalls
Recalled Item: Zzang! Original Candy Bar Recalled by Zingerman's Candy Manufactory Due to...
The Issue: Product recalled due to undeclared soy and milk (butter declared).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Zzang! Wowza Candy Bar Recalled by Zingerman's Candy Manufactory Due to...
The Issue: Product recalled due to undeclared soy; and undeclared milk (cream declared).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...
The Issue: Defective Delivery System: Out of Specification (OOS) results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...
The Issue: Defective Delivery System: Out of Specification (OOS) results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...
The Issue: Defective Delivery System: Out of Specification (OOS) results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Capecitabine tablets USP 500 mg Recalled by Teva North America Due to Failed...
The Issue: Failed Dissolution Specifications: low test results at the 18 month time-point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Life-Line DOCUSATE CALCIUM Sodium Free STOOL SOFTENER 240 mg each Recalled...
The Issue: Labeling: Label mix-up. Docusate Sodium 100mg Softgels were mislabeled as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BARDEX I.C. Anti-Infective 2-Way 3cc Foley Catheter Recalled by C.R. Bard,...
The Issue: Labeling error: Catalog contains Instructions for Use (IFU) error; incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARDEX I.C. Anti-Infective 2-Way Red Latex Foley Catheter Recalled by C.R....
The Issue: Labeling error: Catalog contains Instructions for Use (IFU) error; incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARDEX I.C. Anti-Infective 2-Way 5cc Foley Catheter. Intended for urinary...
The Issue: Labeling error: Catalog contains Instructions for Use (IFU) error; incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fuse 1C Colonoscope Recalled by EndoChoice, Inc. Due to The bending section...
The Issue: The bending section of the device may partially separate from the insertion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mavig Monitor Suspension System Recalled by GE Medical Systems, LLC Due to...
The Issue: GE Healthcare has recently become aware of a reported incident in which a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Aero-AL Impaction handle Catalog Number 48921007. Stryker Spine...
The Issue: Reported jamming of the impaction handle when assembled to the Inserter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeoCoil 3.0T GEM Flex Coil. The 3.0T GEM Flex coil Recalled by NeoCoil, LLC...
The Issue: Potential for higher than specified surface temperatures. Use of 3.0T GEM...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oncentra External Beam - VMAT - Radiation therapy planning system Recalled...
The Issue: When using the option "Tumor Overlap Fraction" in VMAT planning it has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Stryker Color Cuff and Color Cuff II Adult Tourniquet Recalled...
The Issue: Reprocessed Stryker Pressure Tourniquet Cuffs were mislabeled, including...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrex IBalance TKA Tibial Tray Size 2 - Catalog # AR-503-TTTC Recalled by...
The Issue: Devices reported to have a smooth texture to the outer surface of the metal,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadSuite Recalled by Merge Healthcare, Inc. Due to Potential incorrect...
The Issue: Potential incorrect Standardized Uptake Values (SUV) measurements in RadSuite.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView X are gamma cameras Recalled by Philips Medical Systems...
The Issue: The firm discovered four issues with the BrightView Family systems. Issue 1:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT & BrightView XCT Upgrade Recalled by Philips Medical Systems...
The Issue: The firm discovered four issues with the BrightView Family systems. Issue 1:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.