RecallRadar

FDA Device recall Z-0181-2013

AirFlow, Small Adult Resuscitator, AF5000 Series, Single use, Manufactured by: Ventlab Corporation, 155 Boyce Drive, Mockville, NC 27028 Th…

On 2012-11-07 the FDA classified a Class I recall of AirFlow, Small Adult Resuscitator, AF5000 Series, Single use, Manufactured by: Ventlab Corporation, 155 Boyce Drive, Mockville, NC 27028 Th… by Ventlab, citing possible volume leakage through the inlet valve during compressions of the resuscitator bag.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0181-2013
ClassificationClass I
Statusterminated
Initiated2012-07-11
Published2012-11-07
Last updated2026-09-13 11:53 UTC
CompanyVentlab
DistributionUS

Product

AirFlow, Small Adult Resuscitator, AF5000 Series, Single use, Manufactured by: Ventlab Corporation, 155 Boyce Drive, Mockville, NC 27028 The Disposable Resuscitators with optional built-in pressure monitor is intended to provide respiratory support in the presence of reversible apnea, commonly associated with cardiopulmonary arrest.

Reason

Possible volume leakage through the inlet valve during compressions of the resuscitator bag.

Identifiers

code_info
Product Code: AF5140MBPWTD5, Lot #101806 and 102163; AF5140MB-T, Lot #102075 and AFD5140MB-T, Lot #101928 &102211. Reca…Product Code: AF5140MBPWTD5, Lot #101806 and 102163; AF5140MB-T, Lot #102075 and AFD5140MB-T, Lot #101928 &102211. Recall was amended to include the following: AF5140MBS-I, Lot #101898; AF5140MB-ST, Lot #101896; AF5140MBS, Lot #101900 and AF5140MBS-R, Lot #101899.

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-0181-2013%22

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