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 26541–26560 of 27,451 recalls
Recalled Item: Instrumentation Laboratory ACL TOP CTS PN 0000280020 ACL TOP is a bench top...
The Issue: Low Abnormal Fibrinogen Sample Reports as Normal and High Fibrinogen Sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instrumentation Laboratory ACL TOP 700 CTS PN 0000280050 ACL TOP Recalled by...
The Issue: Low Abnormal Fibrinogen Sample Reports as Normal and High Fibrinogen Sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instrumentation Laboratory ACL TOP 500 CTS PN 0000280040 ACL TOP Recalled by...
The Issue: Low Abnormal Fibrinogen Sample Reports as Normal and High Fibrinogen Sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Newport HT70 and HT70 Plus Ventilators Recalled by Newport Medical...
The Issue: May emit a continuous high priority alarm and the ventilator may stop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instrumentation Laboratory ACL TOP (Base) PN 0000280000 ACL TOP is Recalled...
The Issue: Low Abnormal Fibrinogen Sample Reports as Normal and High Fibrinogen Sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medstream 81" (206 cm) 20 Drop Standard bore Universal Administration...
The Issue: Devices leaking at the Y-site
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HALO Flex Energy Generators Manufactured by B¿RRX Medical (now Covidien)...
The Issue: Potential failure of HALO Energy Generator to enter "stand by" mode when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 100 ft roll of tubing inside a cardboard box. Medical Recalled by Steris...
The Issue: On 7/20/2012 the firm became aware that a lot of tubing was distributed by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHADIA Varelisa Cardiolipin IgM Cardiolipin autoantibody immunological test...
The Issue: Customers were not following the labeled assay procedure. This was due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: E-Z WIDER BARIATRIC CHAIR BED Recalled by Kreg Medical Inc. Due to An EZ...
The Issue: An EZ Wider bed (capacity of 1000 lb. safe working load collapsed during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima XR 200 amx with Digital Upgrade. The Recalled by GE...
The Issue: GE Healthcare has become aware of a software issue on the interface of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima XR 220amx 30kw Mobile X-ray System The Recalled by GE...
The Issue: GE Healthcare has become aware of a software issue on the interface of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima XR 220amx 15kw Mobile X-Ray System The Recalled by GE...
The Issue: GE Healthcare has become aware of a software issue on the interface of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DGPHP RFA High-Power Single Use Grounding Pads and Cool-Tip RFA Recalled by...
The Issue: Covidien is conducting a recall of various production lots of DGHP RFA High...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The SYSTEM 1E Liquid Sterilant Processing System. The SYSTEM 1E Recalled by...
The Issue: The firm initiated a recall after complaint investigations revealed that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Custom Implant Devices Packaging: Packaging was not standardized on...
The Issue: In connection with a Warning Letter received from the U.S. Food & Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V60 Ventilator Recalled by Respironics California Inc Due to Respironics is...
The Issue: Respironics is recalling the V60 ventilator because certain blower motor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DEXIS Imaging Suite - catalog number 1.008.7932 Recalled by Imaging Sciences...
The Issue: A condition can occur during renumbering of the patient database using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Emit(R) 2000 Phenobarbital Assay (OSR4D229) and Syva(R) Emit(R)...
The Issue: Firm has confirmed highter imprecision with the recalled lots on Beckman...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multileaf Collimator To be used for single or multiple fractions Recalled by...
The Issue: Information released with the product Agility did not originally contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.