Reported Oct 5, 2022 · Ongoing

MEDLINE CLEARPRO DOUBLE SWIVEL CLOSED SUCTION CATHETER, flat peel pouch EA, 10 EA per Inner Carton (IC), 20 EA/2 Inner…

MEDLINE INDUSTRIES, LP - Northfield

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: MEDLINE INDUSTRIES, LP - Northfield · 3 Lakes Dr · Northfield, IL · 60093-2753

Is this the product you have?

MEDLINE CLEARPRO 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

3 of 3 products

Products covered by this recall
#Product as published
1ET LENGTH DOUBLE SWIVEL, 12 Fr, Item Number/REF: DYNCPDS12
2ET LENGTH DOUBLE SWIVEL, 14 Fr, Item Number/REF: DYNCPDS14
3ET LENGTH DOUBLE SWIVEL, 16 Fr, Item Number/REF: DYNCPDS16
Lot codes and dates

6 of 6 products

Products covered by this recall
#BarcodesProduct as published
120888277703367(01)20888277703367
210888277703360UDI-DI (GTIN) Each: (01)10888277703360, Lot Number 6922040021
320888277703381UDI-DI (GTIN) case: (01)20888277703381
410888277703384UDI-DI (GTIN) Each: (01)10888277703384, Lot Numbers 6921050011, 6921070011, 6921070021, 6921060011, 6921060021, 6921080011, 6921100011, 6921100021, 6921120011, 6922010011, 6922020021, 6922030011
520888277703404UDI-DI (GTIN) case: (01)20888277703404
610888277703407UDI-DI (GTIN) Each: (01)10888277703407, Lot Number 6921120021
Amount recalled
65,320 units

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:34 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.