Invacare Corporation ICCG AC-Powered Adjustable Medical Bed Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
ICCG AC-Powered Adjustable Medical Bed
Brand
Invacare Corporation
Lot Codes / Batch Numbers
Model #''s:1102550, 026757, 720-3M-80PR, IH720-3MQS, IH720-3M, 720-3M-76PR, IH720-2M, IHSC900, 026746, SC900-80P, SC90080L, SC900-76L, 720FULL, IHMC2MFP76, IHMC2MF80, IHMC2MF76, IHMC2MFP76, IHMC3MFP80, IHMC3ZP4I6, IHMC2M3ZP41, IHMC23ZP236, IHMC3SP23, 1H3MRFR76, IH3MRFR80, IH3MR2076, IH3MR2080, IH3MR8FR76, IH3MF8FRU6, IH3MR8FR80, IH3MF8FRU. The serial numbers for the beds affected are as follows: 00Axxxxx thru 00Kxxxxx, 99Axxxxx thru 99Lxxxxx & 98Cxxxxx thru 98Lxxxxx.
Products Sold
Model #''s:1102550, 026757, 720-3M-80PR, IH720-3MQS, IH720-3M, 720-3M-76PR, IH720-2M, IHSC900, 026746, SC900-80P, SC90080L, SC900-76L, 720FULL, IHMC2MFP76, IHMC2MF80, IHMC2MF76, IHMC2MFP76, IHMC3MFP80, IHMC3ZP4I6, IHMC2M3ZP41, IHMC23ZP236, IHMC3SP23, 1H3MRFR76, IH3MRFR80, IH3MR2076, IH3MR2080, IH3MR8FR76, IH3MF8FRU6, IH3MR8FR80, IH3MF8FRU. The serial numbers for the beds affected are as follows: 00Axxxxx thru 00Kxxxxx; 99Axxxxx thru 99Lxxxxx & 98Cxxxxx thru 98Lxxxxx.
Invacare Corporation is recalling ICCG AC-Powered Adjustable Medical Bed due to Component Defect. Metal Oxide Varister (MOV) component of the junction box may short circuit with the potential for device failure.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Component Defect. Metal Oxide Varister (MOV) component of the junction box may short circuit with the potential for device failure.
Recommended Action
Per FDA guidance
The manufacturer notified their distributors of the recall with telephone calls & a letter. The distributors were provided information about the recall and informed of their recall responsibilites.
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