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Terminated

Hudson RCI, Pediatric Nasal Cannula, Non-Flared Prongs, Rx only,

FDA Recall Z-2251-2017 · Posted None

Recalling FirmTeleflex Medical
Recall StatusTerminated
Product CodeCAT
Date Initiated2017-05-09
Date Terminated2025-01-16
Product Quantity1150 units

Reason for Recall

Incorrect labeling; the box label indicates Pediatric, the product insert indicates an Adult device.

Firm Action

Consignees were notified via letter on May 9, 2017.

Root Cause

Unknown/Undetermined by firm

Distribution Pattern

CA, CT, FL, IL, IN, MD, MI, MN, MO, MS, NC, NJ, NY, NV, OH, PA, TX, VA, WI and WV.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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