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. 2,480 recalls have been distributed to Oklahoma in the last 12 months.
Showing 26281–26300 of 49,976 recalls
Recalled Item: MicroScan Pos Combo Panel Type 43 Recalled by Beckman Coulter Inc. Due to...
The Issue: The drug dilution sequence for Moxifloxacin printed on the panel is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minivelle (estradiol transdermal system) 0.1 mg/day Recalled by Noven...
The Issue: Defective Delivery System: no longer meets the specification for shear, an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Minivelle (estradiol transdermal system) 0.0375 mg/day Recalled by Noven...
The Issue: Defective Delivery System: no longer meets the specification for shear, an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ProCair Mattress: (a) PROCAIR PLUS 42X80 Recalled by Joerns Healthcare Due...
The Issue: Joerns Healthcare has identified a potential issue with some of the P.R.O....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Clip Gun Magazines are packaged in individually sealed pouches...
The Issue: The packaging sterile barrier does not comply with the applicable packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARMONIC ACE Shears + Adaptive Tissue Technology Recalled by Ethicon...
The Issue: The devices may have been assembled with an internal component that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Maquet...
The Issue: Ingress of fluids into the device can affect various electronic circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P.R.O. Matt: (a) PROMATT PLUS 36 X 76 MATRESS Recalled by Joerns Healthcare...
The Issue: Joerns Healthcare has identified a potential issue with some of the P.R.O....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARMONIC ACE Shears + Adaptive Tissue Technology Recalled by Ethicon...
The Issue: The devices may have been assembled with an internal component that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smith&nephew ANTHOLOGY POROUS HIGH OFFSET STEM Recalled by Smith & Nephew,...
The Issue: Three lots of Anthology HO Porous size 7 stems were manufactured with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heartware Medtronic HVAD System for cardiac use. Including the following...
The Issue: Possible transient electrical connection interruption between an HVAD System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NaturaLyte¿ Liquid Acid Concentrate for Bicarbonate Dialysis Recalled by...
The Issue: The bottles are mislabeled with an incorrect part number.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MagNA Pure 24 System Recalled by Roche Molecular Systems, Inc. Due to...
The Issue: Cross-contamination of samples has been reported when running the existing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AD-TECH Medical Instrument Corporation Drill Sleeve Guides DSG-6-3-090-2.4N...
The Issue: The diameter of the drill sleeve guide raw material was found to be under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acadica Kratom: Red Hulu 2 Recalled by Badger Botanicals LLC Due to...
The Issue: Recalling Red Suma, Green Suma, Red Hulu 2, Green Hulu 2 Kratom products due...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Acadica Kratom: Red Suma 250g bags Recalled by Badger Botanicals LLC Due to...
The Issue: Recalling Red Suma, Green Suma, Red Hulu 2, Green Hulu 2 Kratom products due...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Acadica Kratom: Green Hulu 2 Kratom Recalled by Badger Botanicals LLC Due to...
The Issue: Recalling Red Suma, Green Suma, Red Hulu 2, Green Hulu 2 Kratom products due...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Acadica Kratom: Green Suma Recalled by Badger Botanicals LLC Due to...
The Issue: Recalling Red Suma, Green Suma, Red Hulu 2, Green Hulu 2 Kratom products due...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Artis Q biplane Recalled by Siemens Medical Solutions USA, Inc Due to After...
The Issue: After the Large Display returns from power save mode, it may not show an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniDiagnost-Eleva X-ray system Angiographic and Diagnostic Recalled by...
The Issue: The fixation of the upper and lower tilt actuator, of the Omnidiagnost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.