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. 2,448 recalls have been distributed to District of Columbia in the last 12 months.
Showing 26801–26820 of 27,451 recalls
Recalled Item: Bayonet Forceps 7.-1/8 (181.0mm) 0.75mm Insulated Tips Recalled by PSC...
The Issue: Firm officials reported to CIN-DO that the outer carton label of this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bayonet Forceps 8.25 (209.6 mm) 0.5mm Tips Recalled by PSC Industries Inc...
The Issue: Firm officials reported to CIN-DO that for this device, in the labeling on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIDEX OPA Recalled by Advanced Sterilization Products Due to The recall was...
The Issue: The recall was initiated because Advanced Sterilization Products has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bayonet Forceps 8.5" (215.9mm) Serrated 1.0 mm Tips...
The Issue: Firm officials reported to CIN-DO that their Electrosurgical Monopolar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Spinal System Lamina Hooks Synthes Medium TI Lamina Hook Recalled...
The Issue: USS Lamina Hooks, Medium, Right are being recalled because the hooks are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT CA 19-9XR Reagent Kit Recalled by Abbott Laboratories Due to The...
The Issue: The six ARCHITECT CA 19-9XR reagent lots are demonstrating a shift up in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult Divided Cannula end tidal C)2 sampling w/male luer-lock connector. 7...
The Issue: A complaint was received, and later verified, that product labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Isothermal Breathing Circuit Recalled by Carefusion 2200 Inc Due to...
The Issue: The Y adapter within the breathing circuit may spontaneously crack, causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Isothermal Breathing Circuit Recalled by Carefusion 2200 Inc Due to...
The Issue: The Y adapter within the breathing circuit may spontaneously crack, causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Isothermal Breathing Circuit Accessory - Infant Patient Y Connector...
The Issue: The Y adapter within the breathing circuit may spontaneously crack, causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasyLink Informatic System is included with the Dimension Vista System....
The Issue: When using the EasyLink Quality Control Package the system may not perform...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRESTLE LUXE¿ Anterior Cervical Plating System Recalled by Alphatec Spine,...
The Issue: On May 9th 2012 Alphatec Spine received a complaint which reported that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: This voluntary medical device correction is related to Alcon products...
The Issue: This medical device correction is related to Alcon products that present a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Horizon Medical Imaging system. Product Usage: Horizon Medical Imaging is...
The Issue: There is a potential to save reports in RadReport with an Incorrect Final...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo(R) Lab Data Manager and syngo(R) Lab Process Manager Recalled by...
The Issue: When using the syngo Quality Control package the system may not perform as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microbiologics 217 Osseo Avenue North Recalled by Microbiologics Inc Due to...
The Issue: Microbiologics is recalling a number of lots of KWIK-QC Gram Stain Slides....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDEV Technologies SUPERA VERITAS Interwoven Self-Expanding Nitinol Stent...
The Issue: There was an error on the outer labeling of this device. The inner label was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trinity Biotech Recalled by Clark Laboratories, Inc. (dba,Trinity Biotech...
The Issue: The Positive Control for the Captia Varicella-Zoster Virus (VZV) IgG Kit has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC unit model 8015 Product Usage: The device is Recalled by...
The Issue: The recall was initiated because the Alaris PC unit model 8015 has a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Advantage CT/PET Fusion for Advantage Windows Workstation with Volume...
The Issue: GE Healthcare has become aware of a potential safety issue due to incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.