Class II — Alliance Tech Medical, Inc
| Recalling firm | ALLIANCE TECH MEDICAL, INC. |
|---|---|
| Registered facility | ALLIANCE TECH MEDICAL, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Completed |
| Reason | Patients have experienced a bad taste associated with the filters. |
| 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 Taiw… |
| Quantity | Approx. 863/100-unit cases |
| Distribution | Distribution was made to AL, AR, AZ, CA, CO, DE, FL, GA, IL, KS, KY, LA, MA, MO, MS, NC, NJ, NY, OH, TN, TX, WA, and WY. There was also distribution to Puerto Rico. Foreign distribution was made to Canada. |
| Initiated | 2014-10-06 |
| Classified | 2019-12-19 |
| Recall number | Z-0714-2020 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Alliance Tech Medical, Inc (Z-0714-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/83830/
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