Data Foundry

Medical device recalls 2022

MEDLINE CLEARPRO TRACH T-PIECE CLOSED SUCTION CATHETER — Class II medical device recall Z-1857-2022

Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2022-10-05, distributed nationwide. Potential for the suction catheter to come apart from the green connector near the thumb valve. The connector

Recall numberZ-1857-2022
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States
Recall initiated2022-08-03
Classified2022-09-29
Reported by FDA2022-10-05
DistributedNationwide (US)
Countries outside the USAE, CA, CL, CO, PA, QA
Quantity136,080 units
UPC / GTIN / UDI-DI10888277703469, 10888277703476, 20888277703466, 20888277703473
Lot numbers6921040012, 6921050011, 6921060011, 6921110011, 6921120011, 6921120012, 6922010011, 6922010012, 6922010031, 6922020031, 6922030011
Model numbersDYNCPTP14, DYNCPTP14T

Product

MEDLINE CLEARPRO TRACH T-PIECE CLOSED SUCTION CATHETER, flat peel pouch EA, 10 EA per Inner Carton (IC), 20 EA/2 Inner cartons per Case (CS). Labeled as follows: a. TRACH T-PIECE, 14 Fr, Item Number/REF: DYNCPTP14; b. TRACH T-PIECE, 14 Fr, Item Number/REF: DYNCPTP14T

Reason for recall

Potential for the suction catheter to come apart from the green connector near the thumb valve. The connector is coming apart from the assembled device when pulling the catheter out of the artificial airway in the patient suctioning process.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1857-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.