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. 2,465 recalls have been distributed to Oklahoma in the last 12 months.
Showing 32701–32720 of 49,976 recalls
Recalled Item: Lamotrigine Orally Disintegrating Tablets (ODT) Recalled by Impax...
The Issue: Labeling; Label Mixup; box labeled to contain 200 mg blister packs but...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lamotrigine Tablets Recalled by Unichem Pharmaceuticals Usa Inc Due to...
The Issue: Tablets/Capsules Imprinted With Wrong ID: incorrect imprint debossed on the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Panoramic X-ray Model PC-1000 Recalled by Panoramic Rental Corp. Due to...
The Issue: Panoramic Corporation is performing a voluntary Medical Device Correction on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System Used to make treatment plans for patients Recalled by...
The Issue: In a specific workflow where contours are edited (enlarged, moved, copied,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HexaPOD evo RT System Product Usage: The intended use of Recalled by Elekta,...
The Issue: Potentially unrecognized incorrect position of the treatment couch in 3D...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amoxicillin For Oral Suspension Recalled by West-Ward Pharmaceuticals Corp....
The Issue: Labeling: Label Error on Declared Strength- bottles missing colored coded...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sagittal Blade 18.0X0.97X90MM Recalled by Stryker Instruments Div. of...
The Issue: Stryker Instruments is voluntarily recalling the Sagittal Blade...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD) Recalled by HeartWare, Inc Due to...
The Issue: Foreign material found within the driveline connector of the HVAD Pump that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Honeywell eyesaline Eyewash Sterile Isotonic Solution Recalled by Sperian...
The Issue: Non Sterility; contaminated with Klebsiella pneumoniae
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DOBUTamine Injection Recalled by Hospira Inc. Due to Discoloration: Firm...
The Issue: Discoloration: Firm received complaints of product discoloration and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pentax Video Gastroscope is intended to be used with a Recalled by Pentax of...
The Issue: PENTAX Medical is initiating this field action to provide customers that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentax Video Colonoscope is intended to be used with a Recalled by Pentax of...
The Issue: Pentax is initiating the product correction of several model numbers of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thermo Scientific QMS Everolimus Assay Recalled by Microgenics Corporation...
The Issue: A reagent stability issue (still under investigation) causes less separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BruxZir Shaded Recalled by Prismatik Dentalcraft, Inc Due to Prismatik...
The Issue: Prismatik Dentalcraft is recalling BruxZir Shaded because the new design was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Fluid Management Set Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Merit Medical Systems, Inc. announces a voluntary field action for Fluid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Connecting Bracket (Fixture) Device (1002.65A0) is designed as a...
The Issue: Post Market Surveillance cases reported to Maquet showing instances in which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vertebral Motion Analyzer (VMA) Recalled by Ortho Kinematics, Inc Due to...
The Issue: Ortho Kinematics, Inc. notified customers of erroneous results of VMA tests...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaPACS versions 8.4.7 Recalled by Novarad Corporation Due to Novarad...
The Issue: Novarad Corporation announces a voluntary field action for the NovaPACS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recalled by Medtronic Inc., Cardiac Rhythm and Heart Failure Due...
The Issue: 78 Viva CRT -Ds and Evera ICDs that were manufactured with a specific subset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recalled by Medtronic Inc., Cardiac Rhythm and Heart Failure Due...
The Issue: 78 Viva CRT -Ds and Evera ICDs that were manufactured with a specific subset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.