Bio-Med Devices, Inc. Pneumotach, Disposable (B) Catalog Number: 4408 Labeled in part: SINGLE USE CATALOG NO.4408 PNEUMOTACH, DISPOSABLE (B) =-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-= CONTENTS: 1- PNEUMOTACH HEAD ASSEMBLY 1- PARATUBE 60'' 2- TUBING FITTINGS 1- 22x22mm ADAPTER Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Pneumotach, Disposable (B) Catalog Number: 4408 Labeled in part: SINGLE USE CATALOG NO.4408 PNEUMOTACH, DISPOSABLE (B) =-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-= CONTENTS: 1- PNEUMOTACH HEAD ASSEMBLY 1- PARATUBE 60'' 2- TUBING FITTINGS 1- 22x22mm ADAPTER
Brand
Bio-Med Devices, Inc.
Lot Codes / Batch Numbers
Lot Numbers: 05092204, 05101104, 05101304, 05101404 05102004, 05102604, 05102804, 05110204 05110304, 05110904, 05111804, 05112404 05120104
Products Sold
Lot Numbers: 05092204, 05101104, 05101304, 05101404 05102004, 05102604, 05102804, 05110204 05110304, 05110904, 05111804, 05112404 05120104
Bio-Med Devices, Inc. is recalling Pneumotach, Disposable (B) Catalog Number: 4408 Labeled in part: SINGLE USE CATALO due to Adapters may be occluded potentially preventing inhalation. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Adapters may be occluded potentially preventing inhalation
Recommended Action
Per FDA guidance
Bio-Med Devices issued recall notifcation by fax on 12/7/04. Accounts are requested to discontine use and return product. A Press Release issued to AP 12/8/04
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026