Masimo RD Set TC-I SpO2 Adult Reusable Ear Sensor, REF: 4053

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    UDI-DI: (01)00843997009904 Lot #: E16JZJ, E16N2C, 17A3A, 17AKM, 17AKN, 17CPV, 17DBE, 17E87, 17E88, 17FAQ, 17GEV, 17J13, 17KBP,17KWZ, 17MDH, 18AEG, 18DCE, 18E04, 18GNZ, 18HKS, 18J35, 18JPH, 18JWM, 18K49, 18KST, 18M03,19BFG, 19CBA, 19D87, 19DZS, 19EAN, 19F47, 19GCW, 19HDJ, 19HTV, 19K3N, 19KAP, 19KPZ, 19M2U,19MKM, 19NRL, 20ABM, 20C76, 20C94, 20DAL, 20FUR, 20G2S, 20HFU, 20KMY, 20KUE, 20MNW, 20NGC,21ASU, 21CBY, 21CTU, 21E08, 21E09, 21EMQ, 21EMR, 21EYS, 21EYT, 21FUF, 21FUG, 21G2S, 21GAG,21JDD, 21JXV, 21K09, 21MAT, 21NEW, 22ADL, 22APR, 22BJM, 22C29, 22D18, 22DRN, 22FHY, 22FYS,22G1W, 22HHW, 22HYW, 22JHE, 22JZX, 22K65, 22M1A, 22M6V, 22MPZ, 22N9G, 22NHZ, 23A2J, 23AAF,23AEX, 23AJG, 23BEN, 23C5X, E20H1H, E21DYW, E21G2N, E21HCQ, E21HMJ, E21HMK, E23CVQ, R17BXM
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Masimo Corporation
Reason for Recall:
TC-I tip clip sensor may produce readings outside the accuracy specification.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

Masimo RD Set TC-I SpO2 Adult Reusable Ear Sensor, REF: 4053

Product Codes/Lot Numbers:

UDI-DI: (01)00843997009904 Lot #: E16JZJ, E16N2C, 17A3A, 17AKM, 17AKN, 17CPV, 17DBE, 17E87, 17E88, 17FAQ, 17GEV, 17J13, 17KBP,17KWZ, 17MDH, 18AEG, 18DCE, 18E04, 18GNZ, 18HKS, 18J35, 18JPH, 18JWM, 18K49, 18KST, 18M03,19BFG, 19CBA, 19D87, 19DZS, 19EAN, 19F47, 19GCW, 19HDJ, 19HTV, 19K3N, 19KAP, 19KPZ, 19M2U,19MKM, 19NRL, 20ABM, 20C76, 20C94, 20DAL, 20FUR, 20G2S, 20HFU, 20KMY, 20KUE, 20MNW, 20NGC,21ASU, 21CBY, 21CTU, 21E08, 21E09, 21EMQ, 21EMR, 21EYS, 21EYT, 21FUF, 21FUG, 21G2S, 21GAG,21JDD, 21JXV, 21K09, 21MAT, 21NEW, 22ADL, 22APR, 22BJM, 22C29, 22D18, 22DRN, 22FHY, 22FYS,22G1W, 22HHW, 22HYW, 22JHE, 22JZX, 22K65, 22M1A, 22M6V, 22MPZ, 22N9G, 22NHZ, 23A2J, 23AAF,23AEX, 23AJG, 23BEN, 23C5X, E20H1H, E21DYW, E21G2N, E21HCQ, E21HMJ, E21HMK, E23CVQ, R17BXM

Distribution:

Nationwide distribution

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1983-2023

Related Recalls