Recall Z-1423-2011 ยท CAW Generator, Oxygen, Portable
Invacare Corporation
HomeFill Oxygen Compressor IOH200 Homefill, The serial numbers are as follows: 10JF034081, 10JF034082, 10JF034083, 10JF034084, 10JF034085, 10JF034086, 10JF034087, 10JF034088, 10JF034089, 10JF034090, 10JF034091, 10JF034092, 10JF034093, 10JF034094, 10JF034095, 10JF034096, 10JF034097, 10JF034098, 10JF034099, 10JF034100, 10JF034101, 10JF034102, 10JF034103, 10JF034104, 10JF034105, 10JF034106, 10JF03410
| Date | Feb 24, 2011 (initiated Jan 11, 2011) |
| Status | Terminated |
| Reason | Invacare Corporation decided to recall the products because risk analysis reveals that inadequate clearance between a motor ground clip and the motor windings may result in an increased risk for shock to service personnel. It also may result in contact with the motor winding, resulting in a shorted winding; this condition has the potential to result in motor failure/shutdown or to cause the motor |
| Root cause | Other |
| Action | The firm, INVACARE Corp., sent an "URGENT PRODUCT RECALL: IOH 200 Homefill Recall" letter dated January 10, 2010 to all customers. The letter described the product, problem and action to be taken by the customers. The customers were instructed to "immediately examine their inventory and quarantine product subject to recall. In addition, if they may have further distributed this product, please identify their customers and notify them at once of this product recall." The customers were also instructed to complete and return an enclosed response form. Note: All product is to be return to the |
| Quantity | 62 Compressors |
| Distribution | Nationwide distribution: USA including states of: FL, GA, KY, LA, MO, NC, NE, NJ and SC. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K003939 | VENTURE HOME FILL II, MODEL IOH 200 Invacare Corp., Mar 21, 2001 |