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. 2,695 recalls have been distributed to Missouri in the last 12 months.
Showing 3741–3760 of 29,298 recalls
Recalled Item: Various Merit Medical convenience kits that contain recalled Jiangsu Shenli...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various Merit Medical convenience kits that contain recalled Jiangsu Shenli...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: HIGH FLOW INSUFFLATION TUBING (with Filter) Model/Catalog...
The Issue: A customer found product with incomplete seals of P/N 20400161S, lot #185198...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SURGICEL FIBRILLAR 1INX2IN(2.5CMX5.1CM) Recalled by Ethicon Sarl, a Johnson...
The Issue: Some foil pouches were found torn open, impacting the sterile barrier which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SURGICEL FIBRILLAR 1INX2IN(2.5CMX5.1CM) Recalled by Ethicon Sarl, a Johnson...
The Issue: Some foil pouches were found torn open, impacting the sterile barrier which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOFIRE FILMARRAY Pneumonia Panel plus Recalled by BioFire Diagnostics, LLC...
The Issue: Pneumonia panels have an increased risk of control failures due to an issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOFIRE FILMARRAY Pneumonia Panel Recalled by BioFire Diagnostics, LLC Due...
The Issue: Pneumonia panels have an increased risk of control failures due to an issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RX Series CYSC- Cystatin C Reagent -Intended for in vitro Recalled by Randox...
The Issue: Cystatin C Reagent marketed without a 510 (k)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OMTech Desktop Laser Engraver Recalled by Rygel Advanced Machines d/b/a...
The Issue: Lack of redundant interlocks, missing required labels and certification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxC 500 AU Clinical Chemistry Analyzer Recalled by Beckman Coulter Mishima...
The Issue: There are two software bug issues with the analyzer. Issue 1: When a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synergetics I-Pack Injection Kit with Drape -For use with Ophthalmic...
The Issue: Could not confirm products were exposed to the proper sterilization cycle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synergetics I Pack Injection Kit Custom-Tray for use with Ophthalmic...
The Issue: Could not confirm products were exposed to the proper sterilization cycle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synergetics I Pack Injection Kit with Wire Speculum- Tray for Recalled by...
The Issue: Could not confirm products were exposed to the proper sterilization cycle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synergetics I Pack Injection Kit- Tray for use with Ophthalmic Recalled by...
The Issue: Could not confirm products were exposed to the proper sterilization cycle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SENSE XL TORSO COIL 1.5T. 16-element receive only coil for Recalled by...
The Issue: Potential for coils to heat up and harm patients (burn).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SENSE XL TORSO COIL 3.0T. 16-element receive only coil for Recalled by...
The Issue: Potential for coils to heat up and harm patients (burn).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SENSE XL TORSO COIL 1.5T Mk2. 16-element receive only coil Recalled by...
The Issue: Potential for coils to heat up and harm patients (burn).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dxl 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...
The Issue: The analyzers were built with nonconforming USB cables made with brass...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zyno Medical Z800 Recalled by Zyno Medical LLC Due to Zyno Medical has found...
The Issue: Zyno Medical has found that certain Z800, Z800F, Z800W, and Z800WF pumps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bag Decanter II Recalled by Microtek Medical Inc. Due to During sterile...
The Issue: During sterile barrier testing performed on the decanter product line, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.