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. 2,480 recalls have been distributed to Oklahoma in the last 12 months.
Showing 23301–23320 of 28,654 recalls
Recalled Item: Tracheopart Set (Right) Recalled by Teleflex, Inc. Due to Customer...
The Issue: Customer complaints reporting that the cobb connector detached from the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchial Double Lumen Tube Set (Left) Recalled by Teleflex, Inc. Due to...
The Issue: Customer complaints reporting that the cobb connector detached from the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchial One Lumen Tube - Right Recalled by Teleflex, Inc. Due to Customer...
The Issue: Customer complaints reporting that the cobb connector detached from the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchial Double Lumen Tube Set (Right) Recalled by Teleflex, Inc. Due to...
The Issue: Customer complaints reporting that the cobb connector detached from the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchial Double Lumen Tube Set (Left) Recalled by Teleflex, Inc. Due to...
The Issue: Customer complaints reporting that the cobb connector detached from the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: White Bronchial Double Lumen Tube Set (Right) Sterile Recalled by Teleflex,...
The Issue: Customer complaints reporting that the cobb connector detached from the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carlens Bronchial Double Lumen Tube Set (Left) Sterile Recalled by Teleflex,...
The Issue: Customer complaints reporting that the cobb connector detached from the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tracheopart Set (Left) Recalled by Teleflex, Inc. Due to Customer complaints...
The Issue: Customer complaints reporting that the cobb connector detached from the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchial One Lumen Tube - Left Recalled by Teleflex, Inc. Due to Customer...
The Issue: Customer complaints reporting that the cobb connector detached from the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Tender I 17/80 10 pieces Product Usage: Intended for Recalled by...
The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Tender I 17/60 10 pieces Product Usage: Intended for Recalled by...
The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK¿ Tender I 13/60 10 pieces Product Usage: Usage: Intended Recalled...
The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Tender I 13/110 10 pieces Product Usage: Intended for Recalled by...
The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Tender II 13/60 10 + 10 pieces Product Usage: Recalled by Roche...
The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phadia 1000 Instrument (introduced as UniCAP 1000) Recalled by Phadia US Inc...
The Issue: During an investigation of instrument logs it was determined that In...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaMap Orion High Resolution Mapping Catheter Recalled by Boston...
The Issue: Some IntellaMap Orion High Resolution Mapping Catheters are exhibiting a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Tender II 13/110 10 + 10 pieces Product Usage: Recalled by Roche...
The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Tender II 17/80 10 + 10 pieces Product Usage: Recalled by Roche...
The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Tender II 13/80 10 + 10 pieces Product Usage: Recalled by Roche...
The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Tender I 17/110 10 pieces Product Usage: Intended for Recalled by...
The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.