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. 2,617 recalls have been distributed to Oklahoma in the last 12 months.
Showing 11121–11140 of 28,654 recalls
Recalled Item: AquaBplus and AquaBplus B2 Water Purification System. For use with Recalled...
The Issue: Incorrectly crimped connectors were installed on the main protective earth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30" (76 cm) Appx 3.3 ml Recalled by ICU Medical, Inc. Due to Potential for...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 26 IN(66 cm) APPX 3.4ml Recalled by ICU Medical, Inc. Due to Potential for...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 42 IN (107 cm) Appx 5.0 ml Recalled by ICU Medical, Inc. Due to Potential...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spiros CLOSED MALE LUER w/RED CAP Recalled by ICU Medical, Inc. Due to...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30" (76 cm) Appx 5.5 mL 20 Drop Admin Set w/Integrated Clave Drip Chamber...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5 IN (13 cm) Appx 1.5 ml Recalled by ICU Medical, Inc. Due to Potential for...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Appx 1.7 ml Bag Spike w/Integrated Clave Recalled by ICU Medical, Inc. Due...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 76 cm (30") Appx 3.3 ml Recalled by ICU Medical, Inc. Due to Potential for...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30" (76 cm) Appx 3.2 ml Recalled by ICU Medical, Inc. Due to Potential for...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spinning Spiros Closed Male Luer Recalled by ICU Medical, Inc. Due to...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 31" (78 cm) Appx 3.4 ml Recalled by ICU Medical, Inc. Due to Potential for...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3mL Syringe w/Spinning Spiros Recalled by ICU Medical, Inc. Due to Potential...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spinning Spiros Recalled by ICU Medical, Inc. Due to Potential for spinning...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AltiVate Reverse Small Socket Insert Recalled by Encore Medical, LP Due to...
The Issue: Product mislabeled. Use may result in a delay in surgery, stopping of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Langston Dual Lumen Catheter. Recalled by Vascular Solutions, Inc. Due to...
The Issue: The inner lumen of the Langston catheter may separate from the hub during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Langston Dual Lumen Catheter Recalled by Vascular Solutions, Inc. Due to The...
The Issue: The inner lumen of the Langston catheter may separate from the hub during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus CHF-CB30S Choledoscope Intended Use: The device was designed to...
The Issue: The CHF-CB30S Device did not have a 510(k) clearance. Additionally, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Langston Dual Lumen Catheter. Recalled by Vascular Solutions, Inc. Due to...
The Issue: The inner lumen of the Langston catheter may separate from the hub during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Langston Dual Lumen Catheter. Recalled by Vascular Solutions, Inc. Due to...
The Issue: The inner lumen of the Langston catheter may separate from the hub during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.