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. 2,590 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,590 in last 12 months

Showing 1552115540 of 49,976 recalls

FoodMay 4, 2021· bloommy Inc.

Recalled Item: "Bloomy*** Biotin Collagen Keratin***Capsules for SKIN Recalled by bloommy...

The Issue: Dietary supplement contains undeclared fish collagen

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodMay 4, 2021· Simkins Brothers Sweets, LLC dba Natural Way Food Group

Recalled Item: Natural Way Almond Butter 16 oz. packaged in clear plastic jars Recalled by...

The Issue: Potential to contain undeclared peanuts

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 4, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH 930 Analyzer with Photometer Lamp (SMN 11075676) Siemens...

The Issue: Photometer Lamp May Reach Saturation Without Flagging Results, may generate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2021· Medtronic Vascular

Recalled Item: Angiographic Guidewire Component: Model Number: 107042 Recalled by Medtronic...

The Issue: The component part numbers intended for shipment to a third-party, where...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
DrugMay 3, 2021· PFIZER, INC

Recalled Item: 0.5% Bupivacaine Hydrochloride Injection Recalled by PFIZER, INC Due to...

The Issue: Labeling: Label Mix-Up: some vials labeled to contain 0.5% Bupivacaine...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 3, 2021· Mylan Institutional LLC

Recalled Item: Thiamine HCl Injection Recalled by Mylan Institutional LLC Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Cartons with the correct...

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

Class III — Low RiskOngoing
Refund
DrugMay 3, 2021· PFIZER, INC

Recalled Item: 1% Lidocaine HCl Injection Recalled by PFIZER, INC Due to Labeling: Label...

The Issue: Labeling: Label Mix-Up: some vials labeled to contain 0.5% Bupivacaine...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 3, 2021· Pfizer Inc.

Recalled Item: Sterile Water for Inj. Recalled by Pfizer Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: particulate matter identified as an insect...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 3, 2021· Ortho-Clinical Diagnostics, INc.

Recalled Item: VITROS CoV2 Ag calibrator (Product Code 6199950) - Product Usage: Recalled...

The Issue: Ortho investigated and confirmed the potential for unexpected failed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft may go unrecognized...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft may go unrecognized...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft may go unrecognized...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft may go unrecognized...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft may go unrecognized...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing