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. 1,757 recalls have been distributed to Missouri in the last 12 months.
Showing 43441–43460 of 52,570 recalls
Recalled Item: SUTUREFIX Ultra S with 1 #2 Ultrabraid (blue) Product Code: Recalled by...
The Issue: Sterility of device is compromised due to breach in sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SUTUREFIX Ultra S with 1 #2 Ultrabraid Suture (blue/white) Product Recalled...
The Issue: Sterility of device is compromised due to breach in sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SUTUREFIX Ultra S Double Loaded Suture Product Code: 72203854 Fastener...
The Issue: Sterility of device is compromised due to breach in sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SUTUREFIX Ultra Anchor XL with one (#2) Ultrabraid Blue Product Recalled by...
The Issue: Sterility of device is compromised due to breach in sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SUTUREFIX Ultra Anchor XL with one (#2) Ultrabraid Cobraid Suture Recalled...
The Issue: Sterility of device is compromised due to breach in sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan WalkAway-40 plus Instrument and MicroScan Walkaway-96 plus...
The Issue: Springs contained in the access door hinge assembly on the Walk Away Plus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Healthcare ADVIA Acid/Base Reagent 1 and 2 Kit containing Recalled...
The Issue: Swollen acid bottles due to a trace metal contamination in the Acid Reagent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSH81 Prosthetic Foot Product Usage: Prosthetic foot for human use Recalled...
The Issue: Ability Dynamics is recalling RUSH81 Prosthetic Foot because the existing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...
The Issue: Additional caution statements have been added to the Instructions For Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...
The Issue: Additional caution statements have been added to the Instructions For Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...
The Issue: Additional caution statements have been added to the Instructions For Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...
The Issue: Additional caution statements have been added to the Instructions For Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...
The Issue: Additional caution statements have been added to the Instructions For Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...
The Issue: Additional caution statements have been added to the Instructions For Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...
The Issue: Additional caution statements have been added to the Instructions For Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...
The Issue: Additional caution statements have been added to the Instructions For Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...
The Issue: Additional caution statements have been added to the Instructions For Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...
The Issue: Additional caution statements have been added to the Instructions For Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KODAK DirectView DR 9000 System Recalled by Carestream Health Inc. Due to A...
The Issue: A control system failure may cause the U-Arm to move downward unexpectedly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur¿ Systems TnI-Ultra assay Recalled by Siemens Healthcare...
The Issue: The solid phase reagent in some of the ADVIA Centaur¿ TnI -Ultra...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.