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. 2,612 recalls have been distributed to District of Columbia in the last 12 months.
Showing 10041–10060 of 27,451 recalls
Recalled Item: VentStar Anesthesia (N) 180 - Drager Breathing Circuits/Anesthesia Sets...
The Issue: Y-piece may become detached from the ventilation hose either before or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Basic (N) 180- Drager Breathing Circuits/Anesthesia Sets Order...
The Issue: Y-piece may become detached from the ventilation hose either before or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Healgen COVID-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma)...
The Issue: Due to two (2) issues: 1) The firm distributed COVID-19 Rapid Test Cassettes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orient Gene COVID- 19 IgG/ IgM Rapid Test Cassette (Whole Recalled by...
The Issue: Due to two (2) issues: 1) The firm distributed COVID-19 Rapid Test Cassettes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Duodenoscope and accessories Recalled by Olympus Corporation of the Americas...
The Issue: Olympus Medical Systems Corporation (OMSC) has received complaints of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit - Product Usage: Used for Continuous Renal Recalled...
The Issue: Variability in the performance of the tubing in the Prismaflex Control Unit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit - Product Usage: Used for Continuous Renal Recalled...
The Issue: Variability in the performance of the tubing in the Prismaflex Control Unit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Preventative Maintenance Kits G5010007) and spare part kits (G5064801 and...
The Issue: Variability in the performance of the tubing in the Prismaflex Control Unit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit - Product Usage: Used for Continuous Renal Recalled...
The Issue: Variability in the performance of the tubing in the Prismaflex Control Unit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TECNIS Toric 1-Piece IOL Recalled by Johnson & Johnson Surgical Vision Inc...
The Issue: Due to the release of nonconforming Intraocular Lenses (IOLs).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensis / Sensis Vibe systems with software version VD12 and Recalled by...
The Issue: System may sporadically freeze (lock-up) during operation or while being in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gram-Negative Bacteria And Associated Resistance Markers Recalled by BioFire...
The Issue: The firm has identified an increased risk of false positive Pseudomonas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioFire BCID2 Panel Recalled by BioFire Diagnostics, LLC Due to The firm has...
The Issue: The firm has identified an increased risk of false positive Pseudomonas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin BIOLOX DELTA MOD HEAD 32mm EX LONG +7mm 12/14 Recalled by Corin Ltd...
The Issue: The size indicated on the labeling on the outer packaging, on the inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin BIOLOX DELTA MOD HEAD 36mm EX LONG +8mm12/14 TAPER. Recalled by Corin...
The Issue: The size indicated on the labeling on the outer packaging, on the inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RNA MEDICAL Recalled by Medline Industries Inc Due to Product was...
The Issue: Product was compromised during shipment.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Digitial Medica X-ray Imagining System Recalled by Shanghai United Imaging...
The Issue: There is a potential for the X-Ray tube head (Touch screen interface) to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACIST Kodama Intravascular Ultrasound Catheter The Kodama Intravascular...
The Issue: Test results from the manufacturing line found a piece of damaged o-ring in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Band Recalled by G & H Wire Company Due to The text on the patient pack is...
The Issue: The text on the patient pack is correct and the product itself remains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Milex Gellhorn Flexible under the following labels: 1) Gellhorn Flexible...
The Issue: The affected Milex Gellhorn pessaries were incorrectly manufactured with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.