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. 2,584 recalls have been distributed to District of Columbia in the last 12 months.
Showing 13101–13120 of 27,451 recalls
Recalled Item: SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Potential for four safety-related software issues impacting systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Confidence Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potential for four safety-related software issues impacting systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoolBlue Hyper-Hypothermia System- body hypothermia system Model: Innercool...
The Issue: Warnings statements have been added- exceeding 40 degree C for extended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blanketrol III Hyper-Hypothermia System- body hypothermia system temperature...
The Issue: Warnings statements have been added- exceeding 40 degree C for extended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blanketrol II Hyper-Hypothermia System Recalled by Cincinnati Sub-Zero...
The Issue: Warnings statements have been added- exceeding 40 degree C for extended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Tina-Quant Myoglobin Gen. 2 Tests system is an immuno-turbidimetric...
The Issue: The firm conducted internal investigations that confirmed customer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QIAsymphony SP SOW 5.0.3 Recalled by Qiagen Sciences LLC Due to QIAsymphony...
The Issue: QIAsymphony software version 5.0.3 - Software issue incorreclty assigns the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151812 Recalled by...
The Issue: Cleaning processes potentially being ineffective
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151811 Recalled by...
The Issue: Cleaning processes potentially being ineffective
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151810 Recalled by...
The Issue: Cleaning processes potentially being ineffective
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151815 Recalled by...
The Issue: Cleaning processes potentially being ineffective
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151813 Recalled by...
The Issue: Cleaning processes potentially being ineffective
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151814 Recalled by...
The Issue: Cleaning processes potentially being ineffective
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: daVinci XI Sureform 60 Reload Recalled by Intuitive Surgical, Inc. Due to...
The Issue: The firm became aware of a manufacturing variation in which black and green...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: daVinci XI Sureform 60 reload Recalled by Intuitive Surgical, Inc. Due to...
The Issue: The firm became aware of a manufacturing variation in which black and green...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Sexual Health Testing Kit Recalled by Privapath Diagnostics Ltd...
The Issue: A supplier informed PrivaPath Diagnostics that there is a potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris EtCO2 Recalled by CareFusion 303, Inc. Due to Calibration; it has...
The Issue: Calibration; it has been determined that the capnographs may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRIVELINE MANAGEMENT SYSTEM 1 DAILY Kit Code: DT18440A - Product Recalled by...
The Issue: Potential for sterile packaging to be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DAILY DRIVELINE KIT Kit Code: DM940 - Product Usage: Kit Recalled by...
The Issue: Potential for sterile packaging to be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIRCUMCISION TRAY Kit Code: CIT2245 - Product Usage: Kit is Recalled by...
The Issue: Potential for sterile packaging to be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.