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. 2,464 recalls have been distributed to District of Columbia in the last 12 months.
Showing 22701–22720 of 27,451 recalls
Recalled Item: Stryker SmartLife Large Aseptic Housing Rx Only The Recalled by Stryker...
The Issue: The SmartLife Aseptic Housings are being recalled in that the top section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RESTORIS PST Straight Shell Inserter An impactor is a reusable Recalled by...
The Issue: MAKO has identified the potential that the shell impactors may be damaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RESTORIS PST Acetabular Straight Shell Impactors An impactor is a Recalled...
The Issue: MAKO has identified the potential that the shell impactors may be damaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Persona Tibial Articular Surface Inserter is a sterilizable instrument...
The Issue: Affected product did not undergo heat treatment hardening step leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mortara Surveyor S12 and Surveyor S19 Patient Monitors. Product Usage:...
The Issue: Martara Instrument, Inc. has recently became aware of a potential safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RESTORIS PST Acetabular Offset Shell Impactors An impactor is a Recalled by...
The Issue: MAKO has identified the potential that the shell impactors may be damaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxC 600i SYNCHRON Access Clinical Analyzer Recalled by Beckman...
The Issue: Beckman Coulter is recalling the Small Form Factor Console PC (SFF PC)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laksell Gamma Knife Perfexion Recalled by Elekta, Inc. Due to Elekta has...
The Issue: Elekta has become aware that the latches may be locked before they have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access 2 Immunoassay Systems Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is recalling the Small Form Factor Console PC (SFF PC)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNIVERSAL Modular Electric/Battery Handpiece for surgery The electric...
The Issue: Non-injury complaints from Europe identified a malfunction that made it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur BNP Assay for in vitro diagnostic use in Recalled by Siemens...
The Issue: Siemens Healthcare Diagnostics has confirmed that approximately 2000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LYFO-DISK Recalled by Microbiologics Inc Due to This strain should be...
The Issue: This strain should be resistant to high levels of Gentamicin and be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KWIK-STIK Recalled by Microbiologics Inc Due to This strain should be...
The Issue: This strain should be resistant to high levels of Gentamicin and be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KWIK-STIK Recalled by Microbiologics Inc Due to This strain should be...
The Issue: This strain should be resistant to high levels of Gentamicin and be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accusorb MRI MAC7010 Product Usage: Radio frequency shielding blankets and...
The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HomeChoice Automated PD system and HomeChoice Pro Automated PD system...
The Issue: There are additional and updated warning and cautions that are not in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accusorb MRI MAC7002 Part Number: MRI-02 MRI-Arm Sleeve Various Sizes...
The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accusorb MRI MAC7001 Part Number: MRI-01 MRI-Large Blanket Various Sizes...
The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accusorb MRI MAC7005 Part Number: MRI-05 Leg Wrap Product Usage: Recalled by...
The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accusorb MRI MAC7008 Part Number: MRI-08 MRI-Boot Product Usage: Radio...
The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.