AB ULAX Merkuriusgatan 8 Motala Sweden 1500 Flex Heat and Moisture Exchanger, Catalog Reference 150 - Product Usage: Heat Moisture Exchangers (HM Es) are designed to enhance humification of ventilator-dependent and non-ventilator dependent patients in critical care, home care and anesthesia. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
1500 Flex Heat and Moisture Exchanger, Catalog Reference 150 - Product Usage: Heat Moisture Exchangers (HM Es) are designed to enhance humification of ventilator-dependent and non-ventilator dependent patients in critical care, home care and anesthesia.
Brand
AB ULAX Merkuriusgatan 8 Motala Sweden
Lot Codes / Batch Numbers
SAP 109381602, Lots 2019-12-20 2020-04-30 2020-05-15 2020-05-20 2020-06-15 2020-06-30
Products Sold
SAP 109381602, Lots: 2018-09-25 2018-11-20 2018-12-10 2018-12-20 2019-01-03 2019-02-20 2019-03-20 2019-04-15 2019-05-30 2019-06-25 2019-08- 15 2019-09-05 2019- 11-05 2019-11-25 *** SAP 109381603, Lots 2019-12-20 2020-04-30 2020-05-15 2020-05-20 2020-06-15 2020-06-30
AB ULAX Merkuriusgatan 8 Motala Sweden is recalling 1500 Flex Heat and Moisture Exchanger, Catalog Reference 150 - Product Usage: Heat Moisture Exchang due to Firm has received 6 complaints that the Heat Moisture Exchanger (HME) disconnected from the closed respiratory circuit during use. If the HME separate. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Firm has received 6 complaints that the Heat Moisture Exchanger (HME) disconnected from the closed respiratory circuit during use. If the HME separates, the ventilator circuit may not provide adequate ventilation to the patient, potentially resulting in lack of oxygen leading to hypoxia or death.
Recommended Action
Per FDA guidance
The firm distributed customer letters dated September 4, 2020, which informed customers of the product issue. Distributors were asked to inform customers of the recall. End users were asked to do the following: Inventory that is Currently In-Use: 1. Please evaluate any currently ventilated patient who may have such a device (any BALLARD Heat Moisture Exchanger (HME) 150) in their airway circuit, to determine if they belong to any of the impacted product lots. 2. If any of your patient(s) do have a potentially impacted device in their airway circuit, you must replace such device with a commercially available alternative as soon as possible. Due to the potential for brain damage or death if a circuit interruption were not noticed for about 4 minutes, this is a critical instruction. If, despite this instruction and at your own discretion , you elect still not to do so, then you must check carefully to ensure that both ends of the device are seated very firmly within the circuit; consider taping the device in place at both ends to avoid any potential for disconnections; and ensure that all alarms are working, monitored and addressed immediately if indicated. 3. Please complete the attached End-User Product Recall Response Form and return a copy of the form by email to: Avanos3250@stericycle.com or fax: (888) 229-0320. 4. Once the form is received, a representative will contact you to facilitate return of impacted BALLARD Heat Moisture Exchanger (HME) 150 . 5. Avanos will manage the return of the impacted BALLARD Heat Moisture Exchanger (HME) 150. Please respond within five (5) business days of receipt of this letter. Inventory Already Consumed 6. Please complete the attached End-User Product Recall Response Form (Attachment 1) and select the appropriate box to indicate that you have no inventory of impacted products. 7. Please return this form to Avanos by either email: Avanos3250@stericycle.com or fax: (888)
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