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. 2,468 recalls have been distributed to Oklahoma in the last 12 months.
Showing 25341–25360 of 28,654 recalls
Recalled Item: Arrow Intra-Aortic Balloon Catheter Kit Fiberoptix (IAB) Recalled by Arrow...
The Issue: Potential for a leak between the catheter and the bifurcate which would...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EOS System X- ray beam Digital radiography system used in Recalled by EOS...
The Issue: EOS imaging discovered during production internal testing that the X-ray...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Optima XR220amx and Optima XR200amx with Digital Upgrade Mobile Recalled...
The Issue: There exists a software issue associated with patient selection from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OrthoPediatrics ACL Reconstruction System is a pediatric and small stature...
The Issue: Part # 01-1008-0040/0047, ACL Sleeve Installation/ Insertion Tool, shipped...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Axillent Debakey Grasping Forceps Recalled by Karl Storz Endoscopy America...
The Issue: KARL STORZ is recalling the Axillent Debakey Grasping Forceps because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE/IMMULITE 1000 Systems FOL Folic Acid Recalled by Siemens Healthcare...
The Issue: potential for an accelerated decline in counts per second (CPS) for three...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Candela Laser GentleLase Pro Recalled by Candela Corporation Due to...
The Issue: Unintended single pulse maybe emitted to handpiece prior to pressing of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Chemistry Systems models 1200 Recalled by Siemens Healthcare...
The Issue: The ADVIA Chemistry software systems using certain software versions allows...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instrument Manager driver : Driver sysu100i that connects to the Recalled by...
The Issue: When connected to the Sysmex UF-100, the Instrument Manager driver sysu100i...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Navigator HD l3F/15F x 46cm Ureteral Access Sheath Set Product No...
The Issue: The 13F/15F Navigator HD Ureteral Access SheathSet are being recalled after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Navigator HD l3F/15F x 36cm Ureteral Access Sheath Set Product No...
The Issue: The 13F/15F Navigator HD Ureteral Access SheathSet are being recalled after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SEAC Advanced Dental System Recalled by ASI Medical, Inc. Due to ASI Medical...
The Issue: ASI Medical is initiating a field correction for the SEAC Advanced Dental...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Navigator HD l3F/15F x 28 cm Ureteral Access Sheath Set Product No...
The Issue: The 13F/15F Navigator HD Ureteral Access SheathSet are being recalled after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand EXCELSIOR SL-10 PRE-SHAPED J 15OCM Recalled by Stryker...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LANX Timberline MPF Lateral Modular Plate Fixation System Straight Split...
The Issue: Lanx, Inc. is recalling various lots of Timberline MPF Straight Split Tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mucus Specimen Trap 40 cc Recalled by Medline Industries Inc Due to There is...
The Issue: There is a potential that the specified mucus specimen traps are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand EXCELSIOR SL-10 PRE-SHAPED C 15OCM Recalled by Stryker...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand EXCELSIOR 1018 PRE-SHAPED 45 150CM Recalled by Stryker...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand COMPLIANT 4MM X 15MM Recalled by Stryker Neurovascular Due to...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand EXCELSIOR SL-10 PRE-SHAPED 90 150CM Recalled by Stryker...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.