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. 2,616 recalls have been distributed to District of Columbia in the last 12 months.
Showing 8641–8660 of 47,654 recalls
Recalled Item: QUADROX-iD Adult Recalled by Maquet Medical Systems USA Due to Product...
The Issue: Product packaging may exhibit small pinholes which may not be visible to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX-iD Pediatric Recalled by Maquet Medical Systems USA Due to Product...
The Issue: Product packaging may exhibit small pinholes which may not be visible to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-HMOD70000-USA/QUADROX-iD Recalled by Maquet Medical Systems USA Due to...
The Issue: 1. An accessory may be improperly placed during packaging, causing creases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX-iR Recalled by Maquet Medical Systems USA Due to 1. An accessory may...
The Issue: 1. An accessory may be improperly placed during packaging, causing creases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX-i Adult Recalled by Maquet Medical Systems USA Due to 1. An...
The Issue: 1. An accessory may be improperly placed during packaging, causing creases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX-i Pediatric Recalled by Maquet Medical Systems USA Due to Product...
The Issue: Product packaging may exhibit small pinholes which may not be visible to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX-i Small Adult Recalled by Maquet Medical Systems USA Due to 1. An...
The Issue: 1. An accessory may be improperly placed during packaging, causing creases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venous Hardshell Cardiotomy Reservoir Recalled by Maquet Medical Systems USA...
The Issue: 1. An accessory may be improperly placed during packaging, causing creases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venous Hardshell Cardiotomy Reservoir Recalled by Maquet Medical Systems USA...
The Issue: Product packaging may exhibit small pinholes which may not be visible to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX-iR Recalled by Maquet Medical Systems USA Due to Product packaging...
The Issue: Product packaging may exhibit small pinholes which may not be visible to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-HMO 71000-USA /QUADROX-i Adult Recalled by Maquet Medical Systems USA...
The Issue: 1. An accessory may be improperly placed during packaging, causing creases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HMOD 70000-USA/QUADROX-iD Adult Recalled by Maquet Medical Systems USA Due...
The Issue: 1. An accessory may be improperly placed during packaging, causing creases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hu Vanilla Crunch Dark Chocolate bar Recalled by HU PRODUCTS Due to...
The Issue: may contain undeclared tree-nuts
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Aeris Balloon Dilation Catheter Recalled by Bryan Medical Inc Due to Mislabeling
The Issue: Devices were mislabeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aptio Automation Storage and Retrieval Module (SRM) Recalled by Siemens...
The Issue: A firmware error may lead to an incorrect association of test result(s) to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Softbed Resuscitaire and/or Birthing Room Warmer with Scale...
The Issue: The Resuscitaire Infant Radiant Warmer with the optional scale could display...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist Device System. a) Monitor 1521US Explore Tech...
The Issue: Medtronic has identified that the logfiles downloaded from the recently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piperacillin and Tazobactam for Injection Recalled by Astral SteriTech...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ampicillin and Sulbactam for Injection Recalled by Astral SteriTech Private...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ceftriaxone for Injection Recalled by Astral SteriTech Private Ltd. Due to...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.