Recalls in Oklahoma (page 34)
3949 recalls.
- Medline Convenience Kits: 1) NEURO SHUNT- CODMAN recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) CHEST/BREAST-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) LVAD DRIVELINE TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) ADMIT KIT recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) DRAPE PACK recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) PPE KIT recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT TRIPLE LUMEN INSERTION recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) DRAPE PACK-CHOICE recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT GENERAL CLOSURE recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) BURN PACK recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) WMC I D PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) LVAD DRIVELINE TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT ACES INSERT PEG recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) TOTE ABRAMS KNEE ARTHROSCOPY recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) DRAWER 6-IV FLUIDS GLOVES recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) LITHOTOMY PACK recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) PLASTIC BIN W/MISC KITS recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) BAPTIST FLOYD ENDO GI KIT recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) MAJOR LAPAROTOMY CDS recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) CHP COCHLEAR SUPPLEMENT CDS recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) DENTAL PACK recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT SURG ONC EXCISION BREAST recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) PICC LINE TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) OPEN HEART CDS recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) OR ARTERIOGRAM recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) ENDO KIT W/SYRINGE recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) BASIC NERVE BLOCK TRAY W/LINEN recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) SCC RF PAIN MGMT recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT STC TRACHEOSTOMY recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) ANCILLARY PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - MONARCH Platform recall (Auris Health, Inc)
Medical deviceClass IIReported February 25, 2026 · Device for bronchoscopic visualization, patient airway access has software issue: if application restarts after patient-side selection, prior to bronchoscope... - Estrone RIA recall (Immunotech A.S.)
Medical deviceClass IIReported February 25, 2026 · The affected Estrone RIA kit lots may rarely give falsely high patient results which might cause Temporary injury of Remote probability. Only in some (very... - Medline Industries IV Administration and Extension Sets: 1) DBD-IV ADMIN SET recall (Medline Industries, LP)
Medical deviceClass IIReported February 25, 2026 · Under circumstances involving exposure to particular chemicals and mechanical forces, the male luer connectors for the specified IV Administration and... - Private Label CVS. Model Number: CVS405406. Helps maintain a moist wound environment recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIReported February 25, 2026 · Potential packaging failures, which could lead to a breach in the sterile barrier. - MEDIHONEY CALCIUM ALGINATE WITH ACTIVE LEPTOSPERMUM HONEY. Model Numbers: recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIReported February 25, 2026 · Potential packaging failures, which could lead to a breach in the sterile barrier. - MediHoney Gel with Active Leptospermum Honey. Model/Catalog Numbers: recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIReported February 25, 2026 · Potential packaging failures, which could lead to a breach in the sterile barrier. - Olympus High Flow Insufflation Unit. Model Number: UHI-3. Used for insufflation of... recall (Olympus Corporation of the Americas)
Medical deviceClass IReported February 25, 2026 · Issue with software algorithm which may lead to overpressure events. - Olympus High Flow Insufflation Unit. Model/ Number: UHI-2. Used for insufflation... recall (Olympus Corporation of the Americas)
Medical deviceClass IReported February 25, 2026 · Issue with software algorithm which may lead to overpressure events. - Olympus High Flow Insufflation Unit. Model Number: UHI. Used for insufflation of... recall (Olympus Corporation of the Americas)
Medical deviceClass IReported February 25, 2026 · Issue with software algorithm which may lead to overpressure events. - SAMIT Youth Multi-Purpose Helmets Recalled Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets; Sold on Amazon by SAMIT Outdoor
Consumer productReported February 19, 2026 · The recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the positional stability and... - Prismatic 3D Prints Recalls Book Nooks Due to Risk of Serious Injury or Death Battery Ingestion; Violates Mandatory Standard for Consumer Products with Coin Batteries and Statute for Battery Packaging
Consumer productReported February 19, 2026 · The recalled book nooks violate the mandatory standard for consumer products containing button cell or coin batteries because the nooks include a spare lithium... - Meijer Recalls Lullaby Lane and MCS Children's Sleepwear Due to Burn Hazard; Violates Mandatory Standard for Children's Sleepwear
Consumer productReported February 19, 2026 · The recalled sleepwear violates the mandatory flammability standard for children's sleepwear, posing a risk of burn injuries to children. - JJGoo LED Balloon Lights Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Button Cell Batteries
Consumer productReported February 19, 2026 · The recalled lights violate the mandatory standard for consumer products containing button cell or coin batteries because they contain button cell batteries... - Joly's Recalls 80% Vinegar Due to Risk of Serious Injury or Death from Poisoning and Chemical Burns; Violates FHSA Labeling Requirements
Consumer productReported February 19, 2026 · The recalled vinegar product violates the precautionary labeling requirements under the Federal Hazardous Substances Act (FHSA) because the hazardous substance... - Huaker Magnetic Balls and Rods Sets Recalled Due to Risk of Serious Injury or Death from Choking; Violates the Small Ball Ban
Consumer productReported February 19, 2026 · The recalled magnet toy building sets violate the mandatory standard for toys because they contain small balls and are intended for children under three years... - Vive Health Recalls Adult Portable Bed Rails Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails
Consumer productReported February 19, 2026 · The recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attached to a bed, users can become entrapped... - Sonic Tots recall (McCain Foods USA Inc)
FoodClass IIReported February 18, 2026 · Foreign material (small hard plastic fragments). - Ore-Ida Tater Tots shaped potatoes recall (McCain Foods USA Inc)
FoodClass IIReported February 18, 2026 · Foreign material (small hard plastic fragments). - Brand Name: Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system... recall (Elekta, Inc.)
Medical deviceClass IIReported February 18, 2026 · Due to an error when defining a new stereotactic reference that users fail to first change an already defined obsolete reference to a pre-plan reference. This... - Brand Name: Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system... recall (Elekta, Inc.)
Medical deviceClass IIReported February 18, 2026 · Due to an error when defining a new stereotactic reference that users fail to first change an already defined obsolete reference to a pre-plan reference. This... - UDENYCA recall (McKesson)
DrugClass IReported February 18, 2026 · Temperature Abuse. 116 cartons with specific serial numbers of Lot 2199821, were stored incorrectly in a controlled room temperature environment instead of the... - Cetrorelix Acetate for Injection recall (Meitheal Pharmaceuticals, Inc)
DrugClass IIReported February 18, 2026 · Defective Delivery System: Missing or duplicated needles within the injection kit - Oxycodone Hydrochloride Tablets recall (Amerisource Health Services LLC)
DrugClass IIReported February 18, 2026 · Defective container: card seal defects (weak/non-existent seals), leading to the tablets falling out of their cavities. - vancomycin HCl recall (Fresenius Kabi Compounding, LLC)
DrugClass IIReported February 18, 2026 · Lack of Assurance of Sterility - vancomycin HCl recall (Fresenius Kabi Compounding, LLC)
DrugClass IIReported February 18, 2026 · Lack of Assurance of Sterility - thiamine HCl recall (Fresenius Kabi Compounding, LLC)
DrugClass IIReported February 18, 2026 · Lack of Assurance of Sterility - ketamine HCl recall (Fresenius Kabi Compounding, LLC)
DrugClass IIReported February 18, 2026 · Lack of Assurance of Sterility - acyclovir sodium recall (Fresenius Kabi Compounding, LLC)
DrugClass IIReported February 18, 2026 · Lack of Assurance of Sterility - Testosterone 100mg Anastrozole 4mg recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter - Testosterone 87.5mg recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter - Testosterone 200mg recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter - Testosterone 100mg recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter - Testosterone 75mg recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter - Testosterone 100mg recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter - Testosterone recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter - Testosterone recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter - Testosterone recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter - Testosterone recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter - Testosterone recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter - Testosterone recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter - Testosterone recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter - Testosterone recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter - Testosterone recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter - Testosterone recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter - ESTRADIOL recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter - ESTRADIOL recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter - ESTRADIOL recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter - ESTRADIOL recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter - ESTRADIOL recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter - ESTRADIOL recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter - ESTRADIOL recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter - ESTRADIOL recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter - ESTRADIOL recall (F.H. INVESTMENTS, Inc. (dba Asteria Health))
DrugClass IIReported February 18, 2026 · Presence of Foreign substance - potential presence of metal particulate matter - Doxazosin Tablets recall (Unichem Pharmaceuticals USA Inc.)
DrugClass IIIReported February 18, 2026 · Tablets/Capsules Imprinted with Wrong ID - Pro Numb Tattoo Numbing Spray recall (Pro Numb Tattoo Numbing Spray LLC)
DrugClass IIReported February 18, 2026 · cGMP deviations - Pro Numb Tattoo Numbing Spray recall (Pro Numb Tattoo Numbing Spray LLC)
DrugClass IIReported February 18, 2026 · cGMP deviations - da Vinci 5 Surgeon Console Viewer Display recall (Intuitive Surgical, Inc.)
Medical deviceClass IIReported February 18, 2026 · Robotic-assisted surgical system has Viewer Display manufactured with outdated firmware, may result in loss of one display-loss of 3D surgical field (depth... - Azurion 5 M20 System Model Numbers: recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported February 18, 2026 · Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active. - Azurion 5 M12 System Model Numbers: recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported February 18, 2026 · Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active. - Azurion 7 M20 System Model Numbers: recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported February 18, 2026 · Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active. - Azurion 7 M12 System Model Numbers: recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported February 18, 2026 · Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active. - Azurion 7 B20 System Model Numbers: recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported February 18, 2026 · Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active. - Azurion 7 B12 System Model Numbers: recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported February 18, 2026 · Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active. - Azurion 3 M15 System Model Numbers: recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported February 18, 2026 · Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active. - Azurion 3 M12 System Model Numbers: recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported February 18, 2026 · Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active. - ATEC Lateral Navigation Disc Prep Instruments LIF NAV recall (Alphatec Spine, Inc.)
Medical deviceClass IIReported February 18, 2026 · Due a design issue where the navigated array connection geometry is incorrect. - ATEC Lateral Navigation Disc Prep Instruments LIF NAV recall (Alphatec Spine, Inc.)
Medical deviceClass IIReported February 18, 2026 · Due a design issue where the navigated array connection geometry is incorrect. - Laerdal Compact Suction Unit 4 RTCA version recall (Laerdal Medical Corporation)
Medical deviceClass IIReported February 18, 2026 · units manufactured in a limited time period may emit electromagnetic noise beyond the acceptable limits for RTCA application specified in RTCA DO-160G Chapter... - Halyard TRANSPORT BAG KIT. Kit Code: LIFE0080-01. recall (AVID Medical, Inc.)
Medical deviceClass IIReported February 18, 2026 · Tyvek bag seal issue which may compromise sterility of the kit. - WB Impression Post Closed Tray incl. guide screw recall (Straumann USA LLC)
Medical deviceClass IIIReported February 18, 2026 · The mix up of the impression caps provided in the package. The provided impression caps are magenta instead of brown.