RecallRadar

FDA Device recall Z-1612-2014

Mucus Specimen Trap 40 cc, Specimen Trap 40 cc with additional transport cap

On 2014-05-21 the FDA classified a Class II recall of Mucus Specimen Trap 40 cc, Specimen Trap 40 cc with additional transport cap by Medline Industries, citing there is a potential that the specified mucus specimen traps are not sterile. Use of the affected products may result in the contamination of patient specimens.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1612-2014
ClassificationClass II
Statusterminated
Initiated2013-11-04
Published2014-05-21
Last updated2026-09-13 11:53 UTC
CompanyMedline Industries
DistributionUS

Product

Mucus Specimen Trap 40 cc, Specimen Trap 40 cc with additional transport cap; Product number DYND44140 (pack of 50), Product number DYND44140H (individual). Mucus Specimen Trap 80 cc, Specimen Trap 80 cc w/ additional transport cap; Product number DYND44180 (pack of 50). Used to collect mucus specimens during suction of fluid from the oral cavity, nose-throat area and/or bronchi of a patient.

Reason

There is a potential that the specified mucus specimen traps are not sterile. Use of the affected products may result in the contamination of patient specimens.

Identifiers

code_infoModel Numbers: DYND44140, DYND44140H, and DYND44180; Purchase Order Number: 4506595929

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1612-2014%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.