CLASS II Device recall · Reported 24 Jun 2015 · FDA Enforcement Report
Viking M, L, and XL Mobile Lifts recalled by Hill-Rom
Hill-Rom is recalling Viking M, L, and XL Mobile Lifts, distributed in 11 states. The recall was initiated on 20 Mar 2015 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-1818-2015
- FDA event ID
- 71132
- Recalling firm
- Hill-Rom, Batesville, IN
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 20 Mar 2015
- FDA classified
- 18 Jun 2015
- Reported
- 24 Jun 2015
- Type
- Voluntary: Firm initiated
- Reason category
- Other Reasons
- Device type
- Wheelchairs, Beds & Lifts
Timeline
| 20 Mar 2015 | Recall initiated by company | |
| 18 Jun 2015 | Classified by FDA | +90 days |
| 24 Jun 2015 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Complaints (including one reported death) allegedly of the lift arm drifting down suddenly. If the lift arm assembly is manually lifted, the actuator can become damaged and get stuck in the highest position. If a patient is lifted into the sling while the actuator is stuck, there is a potential risk of a free fall of the patient, resulting in minor or potentially catastrophic injuries.
Product as listed by the FDA
Viking M, L, and XL Mobile Lifts. Non-AC-powered patient lift.
Where it was distributed
Worldwide Distribution -- AE, AO, AR, AT, AU, AZ, BD, BE, BG, BH, BR, CA, CH, CL, CN, CO, CS, CZ, DE, DK, EG, ES, FI, FR, GR, HK, HR, HU, ID, IE, IL, IN, IQ, IR, IS, IT, JO, JP, KR, KW, LB, LI, LT, LU, LV, MA, MT, MX, MY, NL, NO, NZ, OM, PH, PL, PT, QA, RO, SA, SE, SG, SI, SK, SY, TH, TN, TR, TW, UK, US, VE, and ZA.
ArkansasArizonaCaliforniaColoradoDelawareIdahoIllinoisIndianaMassachusettsMontanaTennessee
Questions about this recall
Why was it recalled?
Complaints (including one reported death) allegedly of the lift arm drifting down suddenly. If the lift arm assembly is manually lifted, the actuator can become damaged and get stuck in the highest position. If a patient is lifted into the sling while the actuator is stuck, there is a potential risk of a free fall of the patient, resulting in minor or potentially catastrophic injuries.
Which lots are affected?
Viking¿ M Lift Model 2040035 (S/N 9 200 000 - 9 201 689) Model 2040015 (S/N 7 500 401 - 7 568 899) Model 2040005 (S/N 7 100 101 - 7 200 200) Viking¿ L Lift Model 2040004 (S/N 7 200 201 - 7 300 300) Viking¿ XL/Viking¿ 300 Lift Model 2040003 (S/N 800 001 - 804 999)
Where was it sold?
Worldwide Distribution -- AE, AO, AR, AT, AU, AZ, BD, BE, BG, BH, BR, CA, CH, CL, CN, CO, CS, CZ, DE, DK, EG, ES, FI, FR, GR, HK, HR, HU, ID, IE, IL, IN, IQ, IR, IS, IT, JO, JP, KR, KW, LB, LI, LT, LU, LV, MA, MT, MX, MY, NL, NO, NZ, OM, PH, PL, PT, QA, RO, SA, SE, SG, SI, SK, SY, TH, TN, TR, TW, UK, US, VE, and ZA.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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