Product Recalls in Missouri
Product recalls affecting Missouri — including food, drugs, consumer products, medical devices, and vehicles distributed to Missouri. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,085 recalls have been distributed to Missouri in the last 12 months.
Showing 13641–13660 of 29,298 recalls
Recalled Item: SOMATOM Definition AS 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: DEMO No Needle Corrugated Carton 30 U/D Recalled by Valeritas, Incorporated...
The Issue: There is a potential for "No Needle Demo Units" to contain a needle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DEMO No Needle Corrugated Carton 20 U/D Recalled by Valeritas, Incorporated...
The Issue: There is a potential for "No Needle Demo Units" to contain a needle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Drive 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: SOMATOM Force 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: SOMATOM Edge Plus 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: 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: 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: 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: 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: 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: SNAG FREE SUTURE TRAY Kit Code: SUT14355 - Product Usage: 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: CIT2650H - 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.
Recalled Item: STERILE FLUORO SSP TRAY Kit Code: MNS11605 - Product Usage: Recalled by...
The Issue: Potential for sterile packaging to be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LVAD DRESSING SYSTEM W/BIOPATCHKit Code: DM700 - Product Usage: Kit Recalled...
The Issue: Potential for sterile packaging to be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEONATAL PICC INSERTION TRAY Kit Code: CVI2310 - Product Usage: Recalled by...
The Issue: Potential for sterile packaging to be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Erisma- LP posterior fixation system with the below specifically affected...
The Issue: Potential for the polyaxial screw to become disassembled during implant.
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.