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. 2,468 recalls have been distributed to Oklahoma in the last 12 months.
Showing 25201–25220 of 28,654 recalls
Recalled Item: Port Kit with Access Infusion Set under the following labels: Recalled by...
The Issue: Navilyst Medical has recalled a Port Kit with Access Infusion Set due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX-Evolution with FF WS These products are permanently installed diagnostic...
The Issue: Carestream Health Inc. has issued a recall for the Carestream DRX-Evolution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HT Connect Peripheral Guide Wire Part Number Description 1012587 018...
The Issue: Abbott Vascular has initiated a recall of the HT Connect Peripheral Guide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synergy XVI The Elekta Synergy S is intended to be Recalled by Elekta, Inc....
The Issue: Potential collision risk when using XVI and external beam shaping devices.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synergy XVI XVI can incorrectly calculate the target position of Recalled by...
The Issue: XVI can incorrectly calculate the target position of the treatment table.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Agility. Version 3.1 of the Integrity interface and control software...
The Issue: During the treatment table, gantry, and collimator calibration procedures,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integrity. Version 1.1 of the Integrity interface and control software...
The Issue: During the treatment table, gantry, and collimator calibration procedures,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Desktop Pro TM linear accelerator control software intended to assist...
The Issue: During the treatment table, gantry, and collimator calibration procedures,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Agility. Version 3.0 of the Integrity interface and control software...
The Issue: During the treatment table, gantry, and collimator calibration procedures,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Viscocel and Viscocel Plus. These products are intraocular fluid devices...
The Issue: CLR Medicals International Inc., initiated a nationwide recall of Viscocel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DR 7500 with FF WS These products are permanently installed Recalled by...
The Issue: Carestream Health Inc. has issued a recall for the Carestream DRX-Evolution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX-Evolution with CSH WS These products are permanently installed...
The Issue: Carestream Health Inc. has issued a recall for the Carestream DRX-Evolution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Abbott m2000sp is an automated system for performing sample Recalled by...
The Issue: The x-drive assembly may fail prematurely. This could cause the manipulator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G1725: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue with...
The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4042LH: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue...
The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4042-2: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue...
The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G1777: Umbilical (2) 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due...
The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G2001: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue with...
The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4043G-2: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue...
The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4043E: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue with...
The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.