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. 2,680 recalls have been distributed to Oklahoma in the last 12 months.
Showing 2241–2260 of 28,654 recalls
Recalled Item: A.L.P.S. mvX-MEDIAL TIBIA PLATE 10H RT-Medial Tibia Plate Recalled by Tyber...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX- Product Name: ANATOMIC LAT FIB PLATE 10H LT Recalled by Tyber...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX- MEDIAL TIBIA PLATE 10H LT- Medial Tibia Plate Recalled by...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 6H RT: Anatomic Lateral Fibula Plate...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 8H LT: Anatomic Lateral Fibula Plate...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX - ANATOMIC LAT FIB PLATE 4H LT: Anatomic Lateral Fibula Plate...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX -ANATOMIC LAT FIB PLATE 4H RT: Anatomic Lateral Fibula Plate...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX- MEDIAL TIBIA PLATE 6H RT-Medial Tibia Plate Recalled by Tyber...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 8H RT: Anatomic Lateral Fibula Plate...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 10H RT- Anatomic Lateral Fibula Plate...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX- MEDIAL TIBIA PLATE 16H LT-Medial Tibia Plate Recalled by Tyber...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX -ANATOMIC LAT FIB PLATE 6H LT- Anatomic Lateral Fibula Plate...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX-P: ANATOMIC LAT FIB PLATE 12H LT- Anatomic Lateral Fibula Plate...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 V4/Masimo Rainbow Sensors: Masimo¿ RD rainbow Adt 8¿ SpCO...
The Issue: Due to an error message that prevents users from utilizing carboxyhemoglobin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 35 ECG cable Recalled by Physio-Control, Inc. Due to Product shipped...
The Issue: Product shipped with incorrect IFU. IFU does not include proper...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microbiologics Multi-Strain Human Papillomavirus (HPV) Control Panel...
The Issue: Internal quality control procedures were not followed correctly for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microbiologics Multi-Strain Human Papillomavirus (HPV) Verification Panel...
The Issue: Internal quality control procedures were not followed correctly for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: HOMEDICS Product Name: Air Compression Leg Massager...
The Issue: Regulatory documentation error and misleading color packaging claim.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M V.A.C. VIA Negative Pressure Wound Therapy System /US Recalled by KCI...
The Issue: Due to increase in complaints related to leak alarms
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Prevena Plus 125 Therapy Unit and System Kits by KCI USA, INC. Due to Due...
The Issue: Due to increase in complaints related to leak alarms
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.