MEDLINE CLEARPRO TRACH DOUBLE SWIVEL CLOSED SUCTION CATHETER — Class II medical device recall Z-1856-2022

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 number	`Z-1856-2022`
Product type	Medical device
Classification	Class II
Status	Ongoing
Voluntary or mandated	Voluntary
Recalling firm	MEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States
Recall initiated	2022-08-03
Classified	2022-09-29
Reported by FDA	2022-10-05
Distributed	Nationwide (US)
Countries outside the US	AE, CA, CL, CO, PA, QA
Quantity	34,920 units
UPC / GTIN / UDI-DI	`10888277703377`, `10888277703391`, `20888277703374`, `20888277703398`
Lot numbers	`6921040012`, `6921070011`, `6921080011`, `6921090011`, `6921100011`, `6921120011`, `6921120021`, `6922030011`, `6922040011`
Model numbers	`DYNCPDS12T`, `DYNCPDS14T`

Product

MEDLINE CLEARPRO TRACH DOUBLE SWIVEL 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 DOUBLE SWIVEL, 12 Fr, Item Number/REF: DYNCPDS12T b. TRACH DOUBLE SWIVEL, 14 Fr, Item Number/REF: DYNCPDS14T

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-1856-2022. 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.