Product Recalls in Oklahoma
Product recalls affecting Oklahoma — including food, drugs, consumer products, medical devices, and vehicles distributed to Oklahoma. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,918 recalls have been distributed to Oklahoma in the last 12 months.
Showing 22241–22260 of 49,976 recalls
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: 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: 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: 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: 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: 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: 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: 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: 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: EGIA45 CT AR MD THK REL Recalled by Covidien LLC Due to The device may be...
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: Pediatric Two-Lumen Central Venous Catheterization Kit with Blue FlexTip...
The Issue: Lidstock contains a labeling error. The lidstock shows the catheter cross...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EGIA 60 CURVED TIP ART 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: SIGNIA TRI-STAPLE 2.0 BLACK 60MM EXTRA THICK RELOA 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: SIGNIA TRI-STAPLE 2.0 CURVED TIP 45MM 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.