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. 2,083 recalls have been distributed to Oklahoma in the last 12 months.
Showing 6281–6300 of 49,976 recalls
Recalled Item: Baxter Seprafilm Adhesion Barrier 1 Half Sheet Recalled by Baxter Healthcare...
The Issue: Product was distributed in the United States without proper regulatory approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision HSI Chronic Catheter Sport Pack 14.5 Fr/Ch (4.8mm)...
The Issue: Products may not be heparin coated as indicated on the label-leads to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision H Chronic Catheter Kit 14.5 Fr/Ch (4.8mm) x Recalled by...
The Issue: Products may not be heparin coated as indicated on the label-leads to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERLA TL 25D SCREW 45 25-S TLF-DS 45 Recalled by SPINEART SA Due to Due to...
The Issue: Due to receiving information regarding difficulties with the insertion of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various Alcon Custom Paks Surgical Procedure Pack containing Oasis 27Ga...
The Issue: Due to complaints of particulates, residue, occlusions, and bent tips for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile surgical convenience kits: a. Medline Cath Lab Special Procedure...
The Issue: Surgical convenience kits containing Pure Pouch component that has weak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile convenience kit: Medline Birthing Room Pack Recalled by MEDLINE...
The Issue: Surgical convenience kits containing Pure Pouch component that has weak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile surgical convenience kit: Medline Retrograde PK-22025203-LF Recalled...
The Issue: Surgical convenience kits containing Pure Pouch component that has weak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prelude Guide Sheath Roadster Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Their is a potential that sheaths labeled with .018 dilators may contain a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-sterile convenience kits: a. Medline CC Drawer 4 IV Circulation Recalled...
The Issue: Surgical convenience kits containing Pure Pouch component that has weak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Keller Funnel 2 Recalled by Allergan Sales, LLC Due to Their is a potential...
The Issue: Their is a potential that breast implants lack the lubricious coating that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Johnson & Johnson VISION Reusable LAMINAR High Flow Irrigation Sleeve...
The Issue: Due to a manufacturing variation of the irrigation sleeves which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prelude Guide Sheath Roadster Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Their is a potential that sheaths labeled with .018 dilators may contain a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile surgical convenience kit: Medline Neuro IR Pack Recalled by MEDLINE...
The Issue: Surgical convenience kits containing Pure Pouch component that has weak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile convenience kits: a. Medline Retrograde PK-22025203-LF Recalled by...
The Issue: Surgical convenience kits containing Pure Pouch component that has weak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-sterile convenience kits: Medline Open Heart CDS Recalled by MEDLINE...
The Issue: Surgical convenience kits containing Pure Pouch component that has weak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-sterile convenience kits: a. Medline Difficult Airway Tray W/O Cook...
The Issue: Surgical convenience kits containing Pure Pouch component that has weak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nonsterile convenience kits: a. Medline Delivery Recalled by MEDLINE...
The Issue: Surgical convenience kits containing Pure Pouch component that has weak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Iron3 - IVD use in the quantitative measurement Recalled by...
The Issue: Potential for falsely elevated Chol_2, LDLC, and Trig_2 results on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: PIEZON Bottle Product Name: PIEZON Bottle Model/Catalog Number:...
The Issue: Received complaints that bottles assembled with one batch of bottle collars...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.