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. 2,438 recalls have been distributed to District of Columbia in the last 12 months.
Showing 34041–34060 of 47,654 recalls
Recalled Item: VITROS 5600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Increased U90-382 or...
The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 350 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 250 Chemistry Systems Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Recalled by Baxter Corporation Englewood Due to All lots of RAPIDFILL...
The Issue: All lots of RAPIDFILL Syringe Strips lack evidence supporting the packaging...
Recommended Action: Stop using. Contact the manufacturer or your 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 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: 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: 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: 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: 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: 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: 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: VP-CH-PNV PRENATAL/POSTNATAL Prescription Folic Acid-Containing Dietary...
The Issue: Defective Delivery System: Product may contain leaking capsules.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ranitidine Syrup (Ranitidine Oral Solution Recalled by Bio-pharm, Inc. Due...
The Issue: Failed Impurities/Degradation Specifications: Product recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or 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: BrightView are gamma cameras Recalled by Philips Medical Systems (Cleveland)...
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.