Data Foundry

Medical device recalls 2019

Alliance Tech Medical — Class II medical device recall Z-0714-2020

Completed recall by Alliance Tech Medical, Inc, reported 2019-12-25, distributed in AL, AR, AZ, CA, CO, DE, FL, GA…. Patients have experienced a bad taste associated with the filters.

Recall numberZ-0714-2020
Product typeMedical device
ClassificationClass II
StatusCompleted
Voluntary or mandatedVoluntary
Recalling firmAlliance Tech Medical, Inc, Granbury, TX, United States
Recall initiated2014-10-06
Classified2019-12-19
Reported by FDA2019-12-25
DistributedAL, AR, AZ, CA, CO, DE, FL, GA, IL, KS, KY, LA, MA, MO, MS, NC, NJ, NY, OH, PR, TN, TX, WA, WY
Countries outside the USCA
Lot numbers130905, 150102
Model numbers100, 7773100/7773000

Product

Alliance Tech Medical, Inc. All Flow Pulmonary Function Filters, 100 filters individually packaged in a clear, sealed bag printed with the part number, 100 filters/box, for single patient use, latex free, box of 100 Reorder Numbers: 5553100 (single filter reorder no. 5553000), 5554100 (single filter reorder no. 5554000), 5555100 (single filter reorder no. 5555000), 5559100 (single filter reorder no. 5559000), 7773100 (single filter reorder no. 7773000), and 7774100 (single filter reorder no. 7774000). The firm name on the label is Alliance Tech Medical, Inc., Granbury, TX, manufactured in Taiwan.

Reason for recall

Patients have experienced a bad taste associated with the filters.

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-0714-2020. 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.