Hitachi Medical Systems America Inc Altaire, Magnetic Resonance Imaging Device. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Altaire, Magnetic Resonance Imaging Device.
Brand
Hitachi Medical Systems America Inc
Lot Codes / Batch Numbers
Serial numbers: L001 to L212
Products Sold
Serial numbers: L001 to L212
Hitachi Medical Systems America Inc is recalling Altaire, Magnetic Resonance Imaging Device. due to The electrical cables that supply gradient power to the magnet can become loose over time and create a potential fire hazard.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The electrical cables that supply gradient power to the magnet can become loose over time and create a potential fire hazard.
Recommended Action
Per FDA guidance
The firm sent a recall/field correction letter, dated 4/11/05, to direct accounts.
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 noticeDistribution
As reported by FDA
AL, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, IL, IN, KS, KY, LA, MI, MN, MS, MO, NE, NV, NJ, NM, NY, NC, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI
Page updated: Jan 10, 2026