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. 2,622 recalls have been distributed to District of Columbia in the last 12 months.
Showing 6841–6860 of 27,451 recalls
Recalled Item: Software : myNeedle Guide 2D license Recalled by Siemens Medical Solutions...
The Issue: In the syngo.CT VA40 and syngo.CT VA50 myNeedle Guide application, the order...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirQ3 Self Pressurizing ILA with Automatic Cuff Inflation and GA Recalled by...
The Issue: There is an orogastric (OG) tube size discrepancy between the labeling in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vasoshield Syringe Packs Recalled by Maquet Cardiovascular, LLC Due to...
The Issue: Ink on the Vasoshield syringe Maquet logo may chip resulting in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemopro 2 with Vasoshield Recalled by Maquet Cardiovascular, LLC Due to...
The Issue: Ink on the Vasoshield syringe Maquet logo may chip resulting in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III Colonovideoscope-For endoscopy and endoscopic surgery within...
The Issue: A single CF-Q180AL colonovideoscope was utilized in a veterinary endoscopy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminos dRF Max with software VE10 Recalled by Siemens Medical Solutions...
The Issue: Potential risk of collision with the ceiling, wall, or objects which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminos Agile Max with software VE10 & VF11- A diagnostic Recalled by...
The Issue: Potential risk of collision with the ceiling, wall, or objects which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uroskop Omnia Max with software VE10 & VF11- A diagnostic Recalled by...
The Issue: Potential risk of collision with the ceiling, wall, or objects which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminos Agile with software VC10 - A diagnostic imaging system Recalled by...
The Issue: Potential risk of collision with the ceiling, wall, or objects which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminos dRF with software VD10- A diagnostic imaging system for Recalled by...
The Issue: Potential risk of collision with the ceiling, wall, or objects which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas SARS-CoV-2 & Influenza A/B Qualitative nucleic acid test for Recalled...
The Issue: The firm received customer complaints regarding false negative Influenza A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas Influenza A/B & RSV UC (Utility Channel) Qualitative nucleic Recalled...
The Issue: The firm received customer complaints regarding false negative Influenza A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas SARS-CoV-2 & Influenza A/B Qualitative assay for use on Recalled by...
The Issue: The firm received customer complaints regarding false negative Influenza A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultracell Wick with 80cc Collection Bag Recalled by Beaver Visitec...
The Issue: Device packaging may contain open seals, compromising product sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CustomEyes kits Recalled by Beaver Visitec International, Inc. Due to Device...
The Issue: Device packaging may contain open seals, compromising product sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RELAY PRO Recalled by Bolton Medical Inc. Due to The product may be shorter...
The Issue: The product may be shorter than packaging indicates
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RELAY PRO Recalled by Bolton Medical Inc. Due to The product may be shorter...
The Issue: The product may be shorter than packaging indicates
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scan Monitor/ScanWatch Recalled by Withings Due to A software bug eliminated...
The Issue: A software bug eliminated the initial ECG activation and review of the ECG...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Nuclear Medicine 600/800 series systems Recalled by GE MEDICAL SYSTEMS...
The Issue: A mitigation may not be correctly implemented. If this is the case, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Nuclear Medicine 600/800 series systems Recalled by GE MEDICAL SYSTEMS...
The Issue: A mitigation may not be correctly implemented. If this is the case, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.