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. 2,566 recalls have been distributed to Oklahoma in the last 12 months.
Showing 18341–18360 of 49,976 recalls
Recalled Item: Tropical Lip Moisturizer Recalled by Yusef Manufacturing Laboratories, LLC...
The Issue: Superpotent Drug: The beginning portion of the batch appears to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Koala Hand Sanitizer Recalled by Beaming White Llc Due to Undeclared Isopropyl
The Issue: Subpotent Drug: active ingredient ethanol tested below label claim and there...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by The Harvard...
The Issue: CGMP Deviation: Potential presence of Nitrosodimethylamine (NDMA) Impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Koala Hand Sanitizer Recalled by Beaming White Llc Due to Undeclared Isopropyl
The Issue: Subpotent Drug: active ingredient ethanol tested below label claim and there...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Koala Hand Sanitizer Recalled by Beaming White Llc Due to Undeclared Isopropyl
The Issue: Subpotent Drug: active ingredient ethanol tested below label claim and there...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clozapine Tablets USP tablet Recalled by Aurobindo Pharma USA Inc. Due to...
The Issue: Presence of foreign tablet: Consumer complaint of Clozapine Tablets 50mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NOW Real Food Raw Macadamia Nuts Unsalted 8 oz retail Recalled by NOW Health...
The Issue: The product tested positive for Salmonella enterica.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Software 1898072 IPC upgrade v 2.7.3.0 - Product Usage: The Recalled by...
The Issue: During internal testing execution of the next generation of Integrated Power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Irinotecan HCL Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to...
The Issue: Defective Container: Customer complaints received of a crimp defect while...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irinotecan HCL Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to...
The Issue: Defective Container: Customer complaints received of a crimp defect while...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nabumetone Tablets Recalled by American Health Packaging Due to Labeling Not...
The Issue: Labeling Not Elsewhere Classified: The statement Pharmacist: Dispense with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nystatin Cream Recalled by Crown Laboratories Due to Subpotent Drug: Out of...
The Issue: Subpotent Drug: Out of specification for assay at the 9-month interval for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aripiprazole Tablets Recalled by Alembic Pharmaceuticals Limited Due to...
The Issue: Labeling: Label mix up: Bottles labeled as aripiprazole 2 mg, 30 count had...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nystatin Cream Recalled by Crown Laboratories Due to Subpotent Drug: Out of...
The Issue: Subpotent Drug: Out of specification for assay at the 9-month interval for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nuvasive NVM5 EMG Module Recalled by NuVasive Inc Due to The NVM5 EMG Module...
The Issue: The NVM5 EMG Module kit intended for intraoperative neurophysiologic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Expansion Control Overlay Recalled by EHOB, Inc. Due to QC inspection...
The Issue: QC inspection observed that a portion of the lot may have been contaminated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enVista one-piece hydrophobic acrylic toric intraocular lens Recalled by...
The Issue: The toric axis marks were misaligned (from the expected position in relation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.8mm Truss Wire Recalled by New Standard Device Inc Due to 1.8mm truss...
The Issue: 1.8mm truss wires are being removed to facilitate the introduction of 2.0mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accurian RF Ablation Recalled by Medtronic Sofamor Danek USA Inc Due to...
The Issue: Insertion difficulty of the probes. The probe was catching on a lip inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accurian RF Ablation Recalled by Medtronic Sofamor Danek USA Inc Due to...
The Issue: Insertion difficulty of the probes. The probe was catching on a lip inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.