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 10881–10900 of 52,570 recalls
Recalled Item: Non-sterile procedural trays labeled as LAPAROSCOPIC Recalled by MEDLINE...
The Issue: Potential for sterile blades, within non-sterile SPT kits containing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-sterile procedural trays labeled as THEDA CLARK TOTAL KNEE CDS Recalled...
The Issue: Potential for sterile blades, within non-sterile SPT kits containing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-sterile procedural trays labeled as ORTHO TRAUMA Recalled by MEDLINE...
The Issue: Potential for sterile blades, within non-sterile SPT kits containing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Procedural Trays Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Sterile blades within sterile kits have the potential for the blade to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-sterile procedural trays labeled as MAJOR/MINOR Recalled by MEDLINE...
The Issue: Potential for sterile blades, within non-sterile SPT kits containing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Procedural Trays Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Sterile blades within sterile kits have the potential for the blade to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Procedural Trays Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Sterile blades within sterile kits have the potential for the blade to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Procedural Trays Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Sterile blades within sterile kits have the potential for the blade to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Programmable Diagnostic Computer Recalled by Siemens Medical Solutions USA,...
The Issue: The firm will be performing a software update to address a software error...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Recalled by Noven...
The Issue: Defective Delivery System: Recalled lot was found to be out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ConvaTec AQUACEL Foam Ag Adhesive Recalled by ConvaTec, Inc Due to ConvaTec...
The Issue: ConvaTec are voluntarily recalling a batch of AQUACEL¿ Foam Ag Adhesive 10cm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTotal Identity Impactor Handle Recalled by Conformis, Inc. Due to Loctite...
The Issue: Loctite thread locker (epoxy) may not have been applied to the screw that is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnipod 5 Automated Insulin Delivery System Product catalog numbers:...
The Issue: The firm has become aware of an issue with the Omnipod 5 Controller where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phenytoin Sodium Injection Recalled by Acella Pharmaceuticals, LLC Due to...
The Issue: Labeling: Not elsewhere classified; the product is being recalled because of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Sulfacetamide 10% Sulfur 4% Cleansing Pads Recalled by Acella...
The Issue: Subpotent drug: Out of specification for assay at the end-of-shelf-life...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenytoin Sodium Injection Recalled by Acella Pharmaceuticals, LLC Due to...
The Issue: Labeling: Not elsewhere classified; the product is being recalled because of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Power-PRO 2 Recalled by Stryker Medical Division of Stryker Corporation Due...
The Issue: Cot may experience unintended motion due to damaged cables. Potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivid S6 ultrasound. Used in ultrasound imaging and analysis in Recalled by...
The Issue: Potential for batteries that have not been replaced at 2 years, as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-CORE 2 Ti Core Recalled by NuVasive Inc Due to Potential that insert will...
The Issue: Potential that insert will be unable to disengage from the vertebral body...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivid i ultrasound. Marketed under the following 510(k) numbers: K033139...
The Issue: Potential for batteries that have not been replaced at 2 years, as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.