RecallRadar

FDA Device recall Z-1622-2020

Philips V60 Ventilators with Power Management PCBA part number 1055906

On 2020-04-08 the FDA classified a Class II recall of Philips V60 Ventilators with Power Management PCBA part number 1055906 by Respironics California, citing solder connection failure on Power Management printed circuit board assembly of ventilators may cause 1) Blower to lose power, spool down, and trigger visual and audible High Prio….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1622-2020
ClassificationClass II
Statusongoing
Initiated2020-03-05
Published2020-04-08
Last updated2026-09-13 11:55 UTC
CompanyRespironics California
DistributionAK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY

Product

Philips V60 Ventilators with Power Management PCBA part number 1055906

Reason

Solder connection failure on Power Management printed circuit board assembly of ventilators may cause 1) Blower to lose power, spool down, and trigger visual and audible High Priority Check Vent alarm indicating a need for alternative ventilation, or 2) Intermittent connection may disrupt expected operation and trigger unexpected shutdown without alarm. Failures may lead to hypercarbia/hypoxemia

Identifiers

code_infoSerial Numbers: 100002908 to 100027093; 100027096 to 100085389; 100085399 to 100109746; 100109868 to 201003390; 201003392 to 201010952

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1622-2020%22

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