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. 1,988 recalls have been distributed to District of Columbia in the last 12 months.
Showing 2501–2520 of 27,451 recalls
Recalled Item: See DocMan Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Custom...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) CATH LAB PACK-LF...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) NEURO BASIN PACK-LF...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable Recalled...
The Issue: Software issues were identified in application version 2.x.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) ENDOSCOPIC SKULL BASE...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC 9800 Fluoroscopic X-Ray System Recalled by GE OEC Medical Systems, Inc...
The Issue: Due to manufacturing issue of insufficient sealing of X-ray tubes and can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: See DocMan Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Custom...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) OPEN HEART CDS-LF...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) ENSEMBLE RACHIS-LF...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) CERVICAL PACK-LF...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: See DocMan Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Custom...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: DEEP BRAIN STIMULATION...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable Recalled...
The Issue: Software issues were identified in application version 2.x.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) VP SHUNT CDS Recalled...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable Recalled...
The Issue: Software issues were identified in application version 2.x.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) MEM MAXILLOFACIAL...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) MICRODISECTOMY PACK...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) NASAL PACK Recalled by...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StatStrip Glucose Hospital Meter System. Model/Catalog Number: 63685....
The Issue: A software bug within the Gen 2 StatStrip Hospital Meter firmware leads to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StatStrip Glucose Ketone (mmol/L) Hospital Meter System. Model/Catalog...
The Issue: A software bug within the meter firmware leads to transmission of erroneous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.