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. 1,020 recalls have been distributed to Missouri in the last 12 months.
Showing 22841–22860 of 52,570 recalls
Recalled Item: Mosaic 310 Bioprosthesis Recalled by Medtronic Inc Due to Mislabeling
The Issue: Fifteen affected devices were distributed worldwide, which were mislabeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRG Salivary Testosterone ELISA- IVD for the detection of Testerone Recalled...
The Issue: Salivary assay may observe a higher percentage of samples with 0 pg/ml...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hancock II T510 Bioprosthesis Recalled by Medtronic Inc Due to Mislabeling
The Issue: Fifteen affected devices were distributed worldwide, which were mislabeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mosaic 310 Bioprosthesis Recalled by Medtronic Inc Due to Mislabeling
The Issue: Fifteen affected devices were distributed worldwide, which were mislabeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hancock II T510 Bioprosthesis Recalled by Medtronic Inc Due to Mislabeling
The Issue: Fifteen affected devices were distributed worldwide, which were mislabeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMIKACIN SULFATE INJECTION Recalled by Heritage Pharmaceuticals, Inc. Due to...
The Issue: Non-Sterility:Microbial growth detected in sub lot of Amikacin Sulfate...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PROCHLORPERAZINE EDISYLATE INJECTION Recalled by Heritage Pharmaceuticals,...
The Issue: Non-Sterility:Microbial growth detected in sub lot of Amikacin Sulfate...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LVivo EF app on Vscan Extend. Sold under the following Recalled by GE...
The Issue: Overestimation bias in automatically calculated ejection fraction (EF)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The device is a 25-gauge infusion line that is part Recalled by Dutch...
The Issue: Labeled 25-gauge surgical pack, TDC Vitrectomy Pack VGPC 25g, containing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Visibly Online Vision Test which is part of Recalled by Opternative Inc...
The Issue: Lack of 510K clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guardian Connect App CSS7200 iOS and Guardian Connect Transmitter GST4C...
The Issue: Customers using the firm's continuous glucose monitoring system application...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge 86-Series-Medical Washer-Disinfector Part Number: S-86682003 Product...
The Issue: Possibility that inlet pump hose of the Washer Disinfector Getinge 86-Series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge 86-Series-Medical Washer-Disinfector Part Number: S-86662003 Product...
The Issue: Possibility that inlet pump hose of the Washer Disinfector Getinge 86-Series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Betamethasone Dipropionate Ointment USP Recalled by Teligent Pharma, Inc....
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Global Pride Rattan Shoots in Brine: 24 oz. glass jar Recalled by U.S. Tov,...
The Issue: New York State Department of Agriculture and Markets sampled and tested...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Laxmi Brand Dried Apricot 7 oz (200g) Plastic Pouch Code: 2324617054...
The Issue: Product contains elevated levels of undeclared Sulfites
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: SIGNIA TRI-STAPLE 2.0 CURVED TIP 60MM MEDIUM/ THIC Recalled by Covidien LLC...
The Issue: The device may be missing one of two pin components that maintain alignment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EGIA 60 ARTICULATING EXTRA THICK SULU Recalled by Covidien LLC Due to The...
The Issue: The device may be missing one of two pin components that maintain alignment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EGIA 60 ARTICULATING MED THICK SULU Recalled by Covidien LLC Due to The...
The Issue: The device may be missing one of two pin components that maintain alignment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EGIA 30 ARTICULATING MED THICK SULU Recalled by Covidien LLC Due to The...
The Issue: The device may be missing one of two pin components that maintain alignment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.