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. 2,642 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,642 in last 12 months

Showing 89418960 of 13,376 recalls

DrugMay 5, 2016· Pharmedium Services, LLC

Recalled Item: 3 mcg/mL Fentanyl Citrate and 0.0625% Bupivacaine HCl (Preservative Free)...

The Issue: Presence of Particulate Matter: API contaminated with glass particulate was...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 5, 2016· Pharmedium Services, LLC

Recalled Item: 6.66 mcg/mL Fentanyl Citrate and 0.22% Bupivacaine HCl (Preservative Free)...

The Issue: Presence of Particulate Matter: API contaminated with glass particulate was...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 5, 2016· KVK-Tech, Inc.

Recalled Item: Benzphetamine Hydrochloride Tablets Recalled by KVK-Tech, Inc. Due to...

The Issue: Discoloration: presence of scuffing marks on tablets.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMay 5, 2016· Pharmedium Services, LLC

Recalled Item: 2 mcg/mL Fentanyl Citrate and 0.2% Bupivacaine HCl (Preservative Free)...

The Issue: Presence of Particulate Matter: API contaminated with glass particulate was...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2016· Fresenius Kabi USA, LLC

Recalled Item: OCTREOTIDE ACETATE INJECTION Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Failed Impuities/Degradation Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2016· Fresenius Kabi USA, LLC

Recalled Item: OCTREOTIDE ACETATE INJECTION Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Failed Impuities/Degradation Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 2, 2016· Sandoz, Inc

Recalled Item: Dicloxacillin Sodium Capsules Recalled by Sandoz, Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications:Out of specification result for...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMay 2, 2016· Sandoz, Inc

Recalled Item: Dicloxacillin Sodium Capsules USP Recalled by Sandoz, Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications:Out of specification result for...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugApril 29, 2016· Making It a Lifestyle

Recalled Item: BLACK LABEL X capsules Recalled by Making It a Lifestyle Due to Undeclared...

The Issue: Marketed without an approved NDA/ANDA - presence of undeclared sildenafil.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugApril 29, 2016· Making It a Lifestyle

Recalled Item: 3rd DEGREE capsules Recalled by Making It a Lifestyle Due to Undeclared...

The Issue: Marketed without an approved NDA/ANDA - presence of undeclared sibutramine.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 29, 2016· Making It a Lifestyle

Recalled Item: BLACK GOLD X ADVANCED capsules Recalled by Making It a Lifestyle Due to...

The Issue: Marketed without an approved NDA/ANDA - presence of undeclared sibutramine.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugApril 28, 2016· Pfizer Inc.

Recalled Item: Zoloft (sertraline HCl) tablets Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Tablet/Capsule Specifications: thick tablets exceeding specifications...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 28, 2016· Lymol Medical

Recalled Item: Sclerosol Intrapleural Aerosol (sterile talc powder) Recalled by Lymol...

The Issue: Defective Delivery System: Defective stem valve causes leakage of the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 27, 2016· Teva North America

Recalled Item: Linezolid Injection Recalled by Teva North America Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: Due to potential for leaking bags.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 27, 2016· Novo Nordisk Inc

Recalled Item: Norditropin FlexPro Somatropin (rDNA origin) injection Recalled by Novo...

The Issue: Defective Delivery System; may have a low frequency assembly fault which may...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 25, 2016· Fresenius Kabi USA, LLC

Recalled Item: Sensorcaine- MPF (Bupivacaine HCI Injection Recalled by Fresenius Kabi USA,...

The Issue: Presence of Particulate Matter: Glass particulate found in sterile...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2016· Dr. Reddy's Laboratories, Inc.

Recalled Item: CVS pharmacy Original Strength Acid Controller tablets Recalled by Dr....

The Issue: Failed impurities/degradation specification: An out of specification results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugApril 20, 2016· Pharmakon Pharmaceuticals, Inc.

Recalled Item: Magnesium Sulfate 50 GM in Lactated Ringers 500 mL bag Recalled by Pharmakon...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 20, 2016· Murray International Trading Co., Inc.

Recalled Item: LARYNGITIS PILLS Herbal Supplement Recalled by Murray International Trading...

The Issue: Marketed Without An Approved NDA/ANDA: Products marked as dietary...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 20, 2016· Pharmakon Pharmaceuticals, Inc.

Recalled Item: Oxytocin 10 Units added to Lactated Ringers in a 500 mL lntravia bag...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund