RecallRadar

FDA Device recall Z-2279-2021

Edwards PediaSat Oximetry Catheter Kit, REF: XT3515SP, Exterior Diameter 5.5F (1.83 mm), Usable Length 15 cm, Number of Lumens 3, Recommend…

On 2021-08-18 the FDA classified a Class II recall of Edwards PediaSat Oximetry Catheter Kit, REF: XT3515SP, Exterior Diameter 5.5F (1.83 mm), Usable Length 15 cm, Number of Lumens 3, Recommend… by Edwards Lifesciences, citing there is a potential for internal leaks within catheters.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2279-2021
ClassificationClass II
Statusterminated
Initiated2021-07-09
Published2021-08-18
Last updated2026-09-13 11:56 UTC
CompanyEdwards Lifesciences
DistributionAZ, CA, FL, IN, MD, MI, NJ, NY, OH, PA, TX, WA

Product

Edwards PediaSat Oximetry Catheter Kit, REF: XT3515SP, Exterior Diameter 5.5F (1.83 mm), Usable Length 15 cm, Number of Lumens 3, Recommended Guidewire Size 0.025" (0.64 mm), Rx Only, Sterile EO, UDI: (01)00690103197532

Reason

There is a potential for internal leaks within catheters.

Identifiers

code_info
LOT NUMBERS: 62685549, 62728569, 62889136, 62903838, 63256058, 62728569, 62889136, 62903838, 62939833, 62452820, 626615…LOT NUMBERS: 62685549, 62728569, 62889136, 62903838, 63256058, 62728569, 62889136, 62903838, 62939833, 62452820, 62661574, 62420335, 62889136, 63256058, 62452820, 62661574, 62685549, 62728569, 62420335, 62420335, 62452820, 62420335, 62452820, 62661574, 62889136, 62903838, 63600994, 63608318, 63608323, 62661574, 62420335, 62661574, 62903838

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2279-2021%22

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