Data Foundry

Medical device recalls 2022

20/30 Priority Pack w/COPILOT — Class II medical device recall Z-0923-2022

Ongoing recall by Abbott Vascular, reported 2022-04-20, distributed nationwide. Due to an increase in complaint trend for leaks and intermittent/loose connections.

Recall numberZ-0923-2022
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmAbbott Vascular, Temecula, CA, United States
Recall initiated2022-03-11
Classified2022-04-13
Reported by FDA2022-04-20
DistributedNationwide (US)
Countries outside the USAE, AR, AU, BE, BR, BS, CA, CH, CL, CN, CO, CR, CZ, DE, DO, ES, FR, GB, GR, ID, IL, IN, IT, JM, JP, KR, LU, MX, NL, NZ, PA, PK, PT, RO, SA, SG, SK, TH, TW, UY, VN, ZA
Quantity131 lots
Reason classespackaging
UPC / GTIN / UDI-DI08717648013973
Lot numbers60308571, 60308572, 60308573, 60308574, 60308575, 60309671, 60309672, 60309673, 60309674, 60309675, 60309676, 60309677, 60309681, 60309682, 60309683, 60309684, 60309685, 60309686, 60309687, 60311341, 60311342, 60311343, 60311344, 60311345, 60312167, 60312168, 60312169, 60312170, 60312171, 60312172, 60312173, 60312174, 60312175, 60312176, 60312177, 60312178, 60313415, 60313416, 60313417, 60313418 and 91 more
Model numbers1003327, WPL2122272-01

Product

20/30 Priority Pack w/COPILOT - REF 1003327 WPL2122272-01 (2019-03-01)

Reason for recall

Due to an increase in complaint trend for leaks and intermittent/loose connections.

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-0923-2022. 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.