Facility
ARJOHUNTLEIGH MAGOG, INC.
1 recall(s) on record — most severe on record: Class II.
| FDA Establishment Identifier (FEI) | 3002655016 |
|---|---|
| Establishment type | Develop Specifications But Do Not Manufacture At This Facility; Manufacture Medical Device |
| Location | 2001 TANGUAY ST. MAGOG Quebec, CA J1X 5Y5 |
| Registration status | Active · expires 2026 |
| Parent company | ARJOHUNTLEIGH AB (owner-operator 9026070) |
| Brand names | SARA LITE; MAXIMOVE; MAXI 500; MAXI SKY 2 PLUS; SARA FLEX; MAXI SKY 2; MAXI LITE; MAXI SKY 1000; MAXI SKY 440; VARIOUS SLINGS AND WALKING JACKET (SPEC. DEVELOPER); MAXI SKY 600; EXTENSION STRAP MAXI SKY 2 |
Devices registered here (1)
- Lift, Patient, Non-Ac-PoweredProduct code FSA · Class I · General Hospital · 21 CFR 880.5510
Recalls & enforcement
- Class IITerminated2013-09-11The lock pin can become stuck in the "in" position during the manual rotation, resulting in the inability to prone a patient
Related
Source: U.S. FDA via openFDA (device registration & enforcement). Data as of 2026-08-13. Verify this facility record at FDA →
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