FDA Device recall Z-0714-2020
Alliance Tech Medical, Inc
- FDA Device
- Class II
- completed
- Published 2019-12-25
On 2019-12-25 the FDA classified a Class II recall of Alliance Tech Medical, Inc by Alliance Tech Medical, citing patients have experienced a bad taste associated with the filters.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0714-2020 |
| Classification | Class II |
| Status | completed |
| Initiated | 2014-10-06 |
| Published | 2019-12-25 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Alliance Tech Medical |
| Distribution | AL, AR, AZ, CA, CO, DE, FL, GA, IL, KS, KY, LA, MA, MO, MS, NC, NJ, NY, OH, PR, TN, TX, WA, WY |
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
Patients have experienced a bad taste associated with the filters.
Identifiers
| code_info | Initial recall - lot number 130905 (all part numbers except 7773100/7773000); second recall - lot number 150102 (part numbers 7773100/7773000 only). |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: completed.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0714-2020%22
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