Liko, Inc.
Franklin, MA
Liko, Inc. appears in FDA device records in Franklin, MA. FDA records list no 510(k) clearances, no PMA records and no registered establishments. As of , FDA records show 12 recalls for this company.
FDA records held for this company
- 510(k) clearances
- 0
- PMA records
- 0
- Recall records
- 12
- Registered establishments
- 0
FDA records under these names
1 nameFDA records resolved to Liko, Inc. carry these names as well, as FDA wrote them. Each is the firm named on a registration, a 510(k), a PMA, a recall or an enforcement report that was joined to this company on a shared FDA identifier or on a matching name.
- Liko North America Increcall
510(k) clearance history
No 510(k) clearance records for this company in the ingested FDA data.
No 510(k) clearance records in the ingested FDA data.
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
No FDA product codes recorded against this company.
Recall records
| Recall | Product | Reason | Classification | Initiated | Status |
|---|---|---|---|---|---|
| Z-0606-2009 | Liko AB Uno Lifts, Powered (non-AC) Patient Lift: Old Uno 102: S/N 20001 through 21300 New Uno 102 EM/EE/ES: S/N 30001 through 48100 Production Dates: Manufactured prior to June 26, 2008 Uno 100 and 102 are battery powered mobile lifts, designed to be used in most of the common lifting situations, for example transfers between bed and wheelchair, to and from the toilet and bathtub or for lifting to and from the floor. | Actuator of the lift has the potential to separate when the upper arm is fully extended. | Terminated | ||
| Z-0605-2009 | Liko AB Uno Lifts, Powered (non-AC) Patient Lift: Uno 100 EM/EE: S/N 7090001 through 7096200 Uno 101: S/N 10001 through 11000 Production Dates: Manufactured prior to June 26, 2008 Uno 100 and 102 are battery powered mobile lifts, designed to be used in most of the common lifting situations, for example transfers between bed and wheelchair, to and from the toilet and bathtub or for lifting to and from the floor. | Actuator of the lift has the potential to separate when the upper arm is fully extended. | Terminated | ||
| Z-1118-2007 | Liko Universal Sling Bar 450 R2R Product NUmber: 3156095 | Sling bar may have a center bolt break at the adapter while in use | Terminated | ||
| Z-1117-2007 | Liko Universal Sling Bar 450 Quick Release Hook (QRH) Product Number: 3156085 | Sling bar may have a center bolt break at the adapter while in use | Terminated | ||
| Z-0791-06 | Liko Universal Slingbar 450 (aluminum) used with the Viking L Patient Lift | The swivel adapter which is mounted directly above the slingbar's split center bolt could be removed and allow the slingbar to be improperly mounted directly into the aluminum link arm. This could cause an unsafe transfer. Patient may fall. | Terminated | ||
| Z-0790-06 | Liko Universal Slingbar 450 (aluminum) used with the Viking M Patient Lift | The swivel adapter which is mounted directly above the slingbar's split center bolt could be removed and allow the slingbar to be improperly mounted directly into the aluminum link arm. This could cause an unsafe transfer. Patient may fall. | Terminated | ||
| Z-0278-06 | SABINA I and SABINA II Patient Lift | Incorrect length leg pin bolts may cause patient lift failures | Terminated | ||
| Z-0277-06 | UNO 102 Patient Lift | Incorrect length leg pin bolts may cause patient lift failures | Terminated | ||
| Z-0276-06 | UNO 100 Patient Lift | Incorrect length leg pin bolts may cause patient lift failures | Terminated | ||
| Z-0877-05 | Sabina I and II EM/EE Patient Lift | Incorrect length support screws may cause patient lift failure | Terminated | ||
| Z-0876-05 | UNO 100 EM/EE Patient Lift | Incorrect length support screws may cause patient lift failure | Terminated | ||
| Z-0875-05 | UNO 102 EM/EE/ES Patient Lift | Incorrect length support screws may cause patient lift failure | Terminated |
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain