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. 2,385 recalls have been distributed to Oklahoma in the last 12 months.
Showing 2101–2120 of 28,654 recalls
Recalled Item: Proxima Drape labeled as UNIVERSAL DAVINCI ROBOTIC P. Sterile surgical...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as HEAD AND NECK OSIS Recalled by MEDLINE INDUSTRIES,...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proxima Drape labeled as FACE LIFT. Sterile surgical drape. Recalled by...
The Issue: Potential breach in pouch packaging which could lead to loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...
The Issue: The potential for devices to fail their self-test as a result of prolonged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: namic convenience kits labeled as: MTS Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: The female luer fittings on the Pressure Monitoring Lines (PMLs) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Z1 Femoral Hip System Recalled by Zimmer, Inc. Due to There is a potential...
The Issue: There is a potential design issue with the Z1 Offset Stem Inserter leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: namic convenience kits labeled as: KIT Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: The female luer fittings on the Pressure Monitoring Lines (PMLs) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: namic convenience kits labeled as: PML Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: The female luer fittings on the Pressure Monitoring Lines (PMLs) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: namic convenience kits labeled as: 1) MTS Recalled by MEDLINE INDUSTRIES, LP...
The Issue: The female luer fittings on the Pressure Monitoring Lines (PMLs) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) CSMC/ABDOMINAL HYST PACK-LF Recalled...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) ACL ARTHROSCOPY PACK Recalled by...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synapse PACS Software Version 7.4.x Recalled by FUJIFILM Healthcare Americas...
The Issue: The incorrect computed patient age is showing in VX for patients less than 3...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) EYE PACK Recalled by MEDLINE...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) ANGIO PACK Recalled by MEDLINE...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) C SECTION Recalled by MEDLINE...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) BREAST PACK-LF Recalled by MEDLINE...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) A & A KNEE PACK-LF Recalled by MEDLINE...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) CLOVIS ROBOTIC-LF Recalled by MEDLINE...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) L S GYN PACK Recalled by MEDLINE...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) C SECTION Recalled by MEDLINE...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.