FDA recall record

Alliance Tech Medical, Inc recall — FDA Z-0714-2020

Patients have experienced a bad taste associated with the filters.

Class IIclassification
Z-0714-2020official record ID
Dec 25, 2019report date

Recall record at a glance

Official recordZ-0714-2020
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusCompleted
Recalling firmAlliance Tech Medical, Inc.
Report dateDec 25, 2019
Recall initiation dateOct 6, 2014
QuantityApprox. 863/100-unit cases
LocationGranbury, TX, United States

Official product description

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.

Why the product was recalled

Patients have experienced a bad taste associated with the filters.

Distribution information

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.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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