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. 2,660 recalls have been distributed to Oklahoma in the last 12 months.
Showing 4881–4900 of 13,376 recalls
Recalled Item: HYDROM 10MG/SUF 200MCG/ML INJ in 20 mL syringe Assurance Infusion Recalled...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FENT 900MCG/SUF 210MCG/ML INJ in 20 mL syringe Assurance Infusion Recalled...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: QUADMIX FORTE in 1 mL vial Assurance Infusion (713) 533-8800 Recalled by...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alprostadil 40 mcg/mL (2 mL vial) Inj. Soln. in 2 Recalled by Assurance...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MORPHINE 10MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TRIMIX 30MG/1MG/10MCG/ML INJ in 5 mL/10 mL vials Assurance Infusion Recalled...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MORPHINE 7MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bi-Mix Forte 30 mg/2 mg/mL Inj. in 1 mL vials Assurance Infusion (713)...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FENTANYL 2000MCG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BUP 7MG/HYDROM 20MG/ML INJ in 20 mL syringe Assurance Infusion (713)...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketorolac Tromethamine Injection Recalled by Hikma Pharmaceuticals USA Inc....
The Issue: Presence of Particulate Matter: particles identified as polydimethylsiloxane...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketorolac Tromethamine Injection Recalled by Hikma Pharmaceuticals USA Inc....
The Issue: Presence of Particulate Matter: particles identified as polydimethylsiloxane...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydrocortisone and Acetic Acid Otic Solution Recalled by Akorn Inc Due to...
The Issue: Subpotent Drug: Low Out of specification (OOS) assay results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NORepinephrine Bitartrate 8 mg added to 250 mL 5% Dextrose Recalled by...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NORepinephrine Bitartrate 4 mg added to 250 mL 5% Dextrose Recalled by...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NORepinephrine Bitartrate 8 mg added to 500 mL 5% Dextrose Recalled by...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Memantine Hydrochloride Extended-release Capsules Recalled by The Harvard...
The Issue: Failed Dissolution Specifications: High out of specification result observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bimatoprost Ophthalmic Solution Recalled by Lupin Pharmaceuticals Inc. Due...
The Issue: Failed Impurities/Degradation Specifications: Out-of-specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estriol [(16a Recalled by Spectrum Laboratory Products Due to Subpotent...
The Issue: Subpotent Drug: Supplier indicated assay results did not meet specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Memantine Hydrochloride Extended-release Capsules Recalled by Lupin...
The Issue: Failed Dissolution Specifications: High out of specification result observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.