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.

49,976 total recalls
2,520 in last 12 months

Showing 2050120520 of 49,976 recalls

DrugOctober 9, 2019· Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Recalled Item: PF-Fentanyl Citrate 2 mcg/mL* & Bupivacaine HCl 0.125% in 0.9% Recalled by...

The Issue: GMP Deviations: potential glass contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2019· Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Recalled Item: PF-Fentanyl Citrate (2 mcg/mL)* & Bupivacaine HCl 0.0625 in 0.9% Recalled by...

The Issue: GMP Deviations: potential glass contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2019· Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Recalled Item: del Nido Cardioplegia Solution Recalled by Nephron Pharmaceuticals...

The Issue: Lack of Assurance of Sterility; bags have potential to leak

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2019· Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Recalled Item: PF-Fentanyl Citrate 2 mcg/mL* & Ropivacaine HCl 0.1% in 0.9% Recalled by...

The Issue: GMP Deviations: potential glass contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2019· Ingenus Pharmaceuticals Llc

Recalled Item: Leucovorin Calcium Injection Recalled by Ingenus Pharmaceuticals Llc Due to...

The Issue: Crystallization: Presence of particulate matter identified as API...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 9, 2019· Stryker Sustainability Solutions

Recalled Item: Zimmer Tourniquet Cuff 30" (Blue) Recalled by Stryker Sustainability...

The Issue: Tourniquet cuffs are potentially mislabeled. If used may lead to (1) Device...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2019· Medivators, Inc.

Recalled Item: Medivators Endo Smartcap Endoscope Tubing. Recalled by Medivators, Inc. Due...

The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2019· Medivators, Inc.

Recalled Item: Medivators Endo carry-on Procedure Kit - Product Usage: Recalled by...

The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2019· Medivators, Inc.

Recalled Item: Medivators EndoGator . Kit for Olympus 140/160/180/190 Series GI Recalled by...

The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2019· Medivators, Inc.

Recalled Item: Medivators EndoGator . Kit for Olympus 140/160/180/190 Series GI Recalled by...

The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2019· Medivators, Inc.

Recalled Item: Medivators Endo Smartcap Endoscope Tubing. Recalled by Medivators, Inc. Due...

The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2019· Medivators, Inc.

Recalled Item: Medivators Endo Smartcap Endoscope Tubing. Recalled by Medivators, Inc. Due...

The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2019· Medivators, Inc.

Recalled Item: Medivators Endo Smartcap Endoscope Tubing. . Packaged as Contents 1 Recalled...

The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2019· Nextremity Solutions

Recalled Item: Stratum Foot Plating System-NL LP Screw 3.5x50mm ST Recalled by Nextremity...

The Issue: Product labeled as STRM-NL-3550ST, NL LP Screw 3.5x50mm ST, lot M1151 may...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2019· Draegar Medical Systems, Inc.

Recalled Item: Infinity M300 telemetry monitoring device Software versions VG2.3.1 and...

The Issue: The devices have potential cybersecurity vulnerabilities, which can include...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: Cobas infinity central lab / cobas infinity core license-a Calculator/Data...

The Issue: Cobasinfinity laboratory solution Version 2.4.1 through Version 2.5.4 Using...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2019· Teleflex Medical

Recalled Item: Arrow EZ-IO Intraosseous Vascular Access System 25mm Needle+Stabilizer Kit...

The Issue: The safety cap attached to needles within the needle sets may become...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2019· Teleflex Medical

Recalled Item: Arrow EZ-IO Intraosseous Vascular Access System 45mm Needle+Stabilizer Kit...

The Issue: The safety cap attached to needles within the needle sets may become...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2019· Teleflex Medical

Recalled Item: Arrow EZ-IO Intraosseous Vascular Access System 15mm Needle+Stabilizer Kit...

The Issue: The safety cap attached to needles within the needle sets may become...

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

Class II — Potential Health HazardOngoing
DrugOctober 7, 2019· Mylan Laboratories Limited (Sterile Products Division)

Recalled Item: Rifampin for Injection Recalled by Mylan Laboratories Limited (Sterile...

The Issue: Failed Impurities/Degradation Specifications: discoloration due to elevated...

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

Class II — Potential Health HazardOngoing
Refund