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. 1,092 recalls have been distributed to Missouri in the last 12 months.
Showing 9161–9180 of 52,570 recalls
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: 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: 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: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...
The Issue: Potential for the labeled sterile ultrasound gel component within packs to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...
The Issue: Potential for the labeled sterile ultrasound gel component within packs to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Always-On Tip Tracked Instruments (SPiN Drive instruments) 19ga ANSO...
The Issue: Electromagnetic (EM) sensor tracking malfunction impacts the use of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...
The Issue: Potential for the labeled sterile ultrasound gel component within packs to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...
The Issue: Potential for the labeled sterile ultrasound gel component within packs to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC 9900 Systems with 9-inch Image Intensifier Recalled by GE OEC Medical...
The Issue: Image intensifiers on systems, used to provide fluoroscopic/digital spot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...
The Issue: Potential for the labeled sterile ultrasound gel component within packs to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...
The Issue: Potential for the labeled sterile ultrasound gel component within packs to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...
The Issue: Potential for the labeled sterile ultrasound gel component within packs to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...
The Issue: Potential for the labeled sterile ultrasound gel component within packs to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...
The Issue: Potential for the labeled sterile ultrasound gel component within packs to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Always-On Tip Tracked Instruments (SPiN Drive instruments) 21ga ANSO...
The Issue: Electromagnetic (EM) sensor tracking malfunction impacts the use of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...
The Issue: Potential for the labeled sterile ultrasound gel component within packs to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Field Upgrade Kits: P/N 5451208 RIU Recalled by GE OEC Medical Systems, Inc...
The Issue: Image intensifiers on systems, used to provide fluoroscopic/digital spot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Probe Cover Kits containing Turkuaz Ultrasound Gel Recalled by...
The Issue: Potential for the labeled sterile ultrasound gel component within packs to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...
The Issue: Potential for the labeled sterile ultrasound gel component within packs to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.