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. 2,520 recalls have been distributed to Oklahoma in the last 12 months.
Showing 20161–20180 of 49,976 recalls
Recalled Item: Apollo EZ Recalled by Villa Sistemi Medicali S.P.A. Due to An amendment to...
The Issue: An amendment to the IFU and Service Manual is being issued to prescribe the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo DRF Recalled by Villa Sistemi Medicali S.P.A. Due to An amendment to...
The Issue: An amendment to the IFU and Service Manual is being issued to prescribe the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo Recalled by Villa Sistemi Medicali S.P.A. Due to An amendment to the...
The Issue: An amendment to the IFU and Service Manual is being issued to prescribe the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ascension¿ Silicone PIP-Silicone PIP Sz 1 Recalled by Integra Lifesciences...
The Issue: Silicone PIP Implant mislabeled as a size 1 implant on the outer packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Healix Knotless ADV BR 4.75 Suture Anchor Recalled by DePuy Mitek, Inc., a...
The Issue: Specific product codes and lots of the Mitek HEALIX ADVANCE" Knotless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Healix Knotless ADV BR 5.5 Suture Anchor Recalled by DePuy Mitek, Inc., a...
The Issue: Specific product codes and lots of the Mitek HEALIX ADVANCE" Knotless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Site~Rite 8 Ultrasound Systems-intended for diagnostic ultrasound imaging of...
The Issue: The indicator may show available charge when the battery is close to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 80003 Broccoli Chedder Pasta Salad Kit 2/2.8125 LBS Distributed by: Recalled...
The Issue: Potential to be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 3570 Mix Recalled by Vinyard Fruit & Vegetable Co., Inc. Due to Potential...
The Issue: Potential to be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 3536 Mix Recalled by Vinyard Fruit & Vegetable Co., Inc. Due to Potential...
The Issue: Potential to be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 3582 Mix Recalled by Vinyard Fruit & Vegetable Co., Inc. Due to Potential...
The Issue: Potential to be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 3021 BROCCOLI FLORETS 3LB Recalled by Vinyard Fruit & Vegetable Co., Inc....
The Issue: Potential to be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 7109 Veg Kit Recalled by Vinyard Fruit & Vegetable Co., Inc. Due to...
The Issue: Potential to be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 3512 CALIFORNIA MEDLEY packaged in plastic flexible bags Recalled by Vinyard...
The Issue: Potential to be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ranitidine Syrup (Ranitidine Oral Solution USP) Recalled by American Health...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydrocodone Bitartrate and Homatropine Methlybromide Oral Solution 5 mg/1.5...
The Issue: Presence of Foreign Substance: Black particles were found in the lots during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BioPlex 2200 ANA Screen Control Set Recalled by Bio-Rad Laboratories, Inc....
The Issue: A new lot of ANA screen control and any subsequent control lots are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LETS GEL KIT Convenience Pack (To prepare 100 mL LETS GEL) Recalled by...
The Issue: Microbial contamination of non-sterile product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Leader Advanced Probiotic with 6 Probiotic Strains and 20 billion Recalled...
The Issue: Incorrect Probiotic blend indicated in the Supplemental Facts Panel on...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Potassium Phosphate Recalled by Avantor Performance Materials Inc Due to...
The Issue: Failed Stability Specifications: Product exceeds compendia and firm's...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.