- Recalling firm
- Draeger, Inc.
- Reason for recall
- Potential cracks in the hose, which could lead to leakage or the hose falling off.
- Affected products (lot / model / serial)
- Part Number MP00310. UDIDI: 04048675422358. All lot numbers.
- Units affected
- 1,063,643 units
- Distribution pattern
- US Nationwide distribution including in the states of IN, AK, AL, AZ, CA, CO, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MI, MN, MO, NC, ND, NE, NH, NJ, NY, OH, OK, OR, PA, RI, SD, TN, TX, VT, WA, WI, WV, WY, MS, SC, UT, VA, AR, and territories AS and PR. The countries of Canada, Germany, United Kingdom, Spain, Italy, Ireland, Poland, Australia, Switzerland, Netherlands, Portugal, France, Austria, Hong Kong, Malaysia, Costa Rica, Andorra, Belgium, Sweden, Cyprus, Greece, Latvia, Romania, Albania, Moldavia, Kazakhstan, Croatia, Libya, Mauritius, Honduras, Suriname, Uruguay, Syria, Israel, Kuwait, Bahrain, Qatar, Utd.Arab.Emir., Oman, Denmark, Norway, New Zealand, Brunei Darussalam, Singapore, China, India, Japan.
- Firm location
- Telford, PA, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- E-Mail
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-3252-2026
- Recall initiated
- September 3, 2026
- FDA classification date
- September 30, 2026
- FDA report date
- October 7, 2026
- FDA event ID
- 99787
- Last updated on HTM Vibe
- October 13, 2026
