CLASS II Device recall · Reported 24 Oct 2018 · FDA Enforcement Report
Multirall(TM) 200Liko Strap Gripper recalled by Liko AB
Liko AB is recalling Multirall(TM) 200Liko Strap Gripper, distributed in Ohio. The recall was initiated on 17 Jul 2018 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-0105-2019
- FDA event ID
- 80911
- Recalling firm
- Liko AB, Lulea, N/A
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 17 Jul 2018
- FDA classified
- 12 Oct 2018
- Reported
- 24 Oct 2018
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Other Reasons
- Device type
- Masks, Gloves & PPE
Timeline
| 17 Jul 2018 | Recall initiated by company | |
| 12 Oct 2018 | Classified by FDA | +87 days |
| 24 Oct 2018 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
The products manufactured on 5/5/17 may be assembled incorrectly. If the incorrectly assembled products is used for patient transport, this could allow the patient to fall, resulting in potential injury to the patient.
Product as listed by the FDA
Multirall(TM) 200Liko Strap Gripper P/N 3136250 overhead lift for patient transfer situations.
Where it was distributed
The products were distributed to the following US states: OH.
Questions about this recall
Is Multirall(TM) 200Liko Strap Gripper recalled?
Yes. Liko AB recalled Multirall(TM) 200Liko Strap Gripper on 17 Jul 2018. The recall is Class II and its status is Terminated. Recall number Z-0105-2019.
Why was it recalled?
The products manufactured on 5/5/17 may be assembled incorrectly. If the incorrectly assembled products is used for patient transport, this could allow the patient to fall, resulting in potential injury to the patient.
Which lots are affected?
Part Number 3136250, the manufacturing date is on the right side of the label listed as 2017-05-05.
Where was it sold?
The products were distributed to the following US states: OH.
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 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other Masks, Gloves & PPE recalls
All 447| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | P28 Phanton Intramedullary Nail System recalled by Paragon 28 | Paragon 28 | Sterility | Nationwide |
| Device | CLASS II | Cyberknife Treatment Deliver System equipped recalled | Accuray Incorporated | Device Malfunction | Nationwide |
| Device | CLASS II | Adapter for Head Positioning recalled by Baxter Healthcare | Baxter Healthcare | Other | Nationwide |
| Device | CLASS II | Cyberknife Treatment Deliver System equipped recalled | Accuray Incorporated | Device Malfunction | Nationwide |
| Device | CLASS II | Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference recalled | O&m Halyard | Other | Nationwide |