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. 2,576 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,576 in last 12 months

Showing 1680116820 of 49,976 recalls

Medical DeviceDecember 1, 2020· Biomet, Inc.

Recalled Item: Vanguard 360 Revision System Posterior Augment With Bolt - Product Recalled...

The Issue: Incorrect bolt -tibial bolts in package instead of femoral bolts may delay...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/ zeego & Artis Q/ Q.zen Artis Pheno Recalled by Siemens Medical...

The Issue: When the user changes frame rates from lower frequency (e.g. 10 f/s) to...

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

Class II — Potential Health HazardOngoing
DrugNovember 25, 2020· US Compounding Inc

Recalled Item: Neostigmine Methylsulfate PF Inj. 5 mg/5 mL Recalled by US Compounding Inc...

The Issue: Labelling: Missing label.

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

Class III — Low RiskOngoing
Refund
DrugNovember 25, 2020· Torrent Pharma Inc

Recalled Item: Anagrelide Capsules Recalled by Torrent Pharma Inc Due to Failed Dissolution...

The Issue: Failed Dissolution Specifications

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: 3.0mm Cannulated Screw System Recalled by Biomet, Inc. Due to Specific lots...

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: Comprehensive Total Shoulder System/Bio-Modular Choice Shoulder System...

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: Oxford Fixed Lateral Recalled by Biomet, Inc. Due to Specific lots of...

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: Custom Cancellous Thread Recalled by Biomet, Inc. Due to Specific lots of...

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: Sterile Trac System Thinflap 24 MM Burr Hole Plate Recalled by Biomet, Inc....

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: PHOENIX Recalled by Biomet, Inc. Due to Specific lots of multiple sterile...

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: M/H MODULAR STEM Recalled by Biomet, Inc. Due to Specific lots of multiple...

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: OSS Polyethylene Tibial Bushing Recalled by Biomet, Inc. Due to Specific...

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: RINGLOC BIPOLAR Hip System Bi Polar Locking Ring Recalled by Biomet, Inc....

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: Comprehensive Reverse Shoulder System Recalled by Biomet, Inc. Due to...

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: 4.0/5.0mm Cannulated Screw System Recalled by Biomet, Inc. Due to Specific...

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: RINGLOC ACETABULAR SYSTEM Self-tapping bone screws Recalled by Biomet, Inc....

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: 6.5/8.0mm Cannulated Screw System Recalled by Biomet, Inc. Due to Specific...

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: Titanium IFS Recalled by Biomet, Inc. Due to Specific lots of multiple...

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: RingLoc+ Quick Connect Drill Bit Recalled by Biomet, Inc. Due to Specific...

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: RapidFire Clip Recalled by Biomet, Inc. Due to Specific lots of multiple...

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing