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. 1,070 recalls have been distributed to Oklahoma in the last 12 months.
Showing 15661–15680 of 49,976 recalls
Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...
The Issue: There is a potential for the screw blocking mechanism on the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...
The Issue: There is a potential for the screw blocking mechanism on the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...
The Issue: There is a potential for the screw blocking mechanism on the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Concerto User Interface Software provided with the following systems: (1)...
The Issue: If a saved treatment plan with 2 opposing beams is edited prior to approval,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...
The Issue: There is a potential for the screw blocking mechanism on the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...
The Issue: There is a potential for the screw blocking mechanism on the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NES Reprocessed Visions PV .035 IVUS Catheter Recalled by Northeast...
The Issue: 510k indicated one (1) reprocessing cycle, product not cleared for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...
The Issue: There is a potential for the screw blocking mechanism on the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...
The Issue: There is a potential for the screw blocking mechanism on the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...
The Issue: There is a potential for the screw blocking mechanism on the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GS777 Wall Transformer Model: 77710 Intended Use: The GS777 Wall Recalled by...
The Issue: Potential Risk of fluid ingress to the power supplies, resulting in risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProBP 3400 Digital Blood Pressure Device ((handheld Recalled by Welch Allyn...
The Issue: Potential Risk of fluid ingress to the power supplies, resulting in risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Bile Esculin Azide Agar w/ 6mcg/ml Vancomycin Recalled by Remel Inc...
The Issue: The media allows growth of E. faecalis ATCC 29212 with blackening of the media.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enoki Mushroom Product of Korea Net Wt. 200 g/7.05 oz. Recalled by GOLDEN...
The Issue: Michigan Department of Agriculture and Rural Development sampled product and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VIA Microcatheter VIA 17 - Product Usage: is Recalled by MICROVENTION INC....
The Issue: Due to inadvertently shipping to U.S. customers with international labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rubber Dam Clamp Recalled by Dentech Corp. Due to Removing parts for safety...
The Issue: Removing parts for safety reasons due to possible breakage.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIA Microcatheter VIA 21 - Product Usage: is Recalled by MICROVENTION INC....
The Issue: Due to inadvertently shipping to U.S. customers with international labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentax Medical Video Duodenoscope - Product Usage: intended to be Recalled...
The Issue: IFU updated: The warning section of the IFU for both the OE-A63 distal end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation (Treatment Planning System) Model Number RayStation is 6.0.0.24...
The Issue: Evaluation of a clinical goal for the voxelwise worst dose distributions may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELUVIA Drug-Eluting Vascular Stent System - Product Usage: indicated for...
The Issue: One batch of the ELUVIATM Drug Eluting Vascular Stent System incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.