ErgoSafe Products, LLC (DBA) Prism Medical

FDA Regulatory Profile

ErgoSafe Products, LLC (DBA) Prism Medical appears in FDA public data with 7 recalls, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1406-2017, Class II) was initiated on January 30, 2017.

Summary

Total Recalls
7
510(k) Clearances
0
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-1406-2017Class IIA-series lift - A625 Manual Part No. 324117. Prism Medical.January 30, 2017
Z-1405-2017Class IIA-series lift - A625 Manual w/Load Cell & Wi-Fi, Omni Part No. 324124. Prism Medical.January 30, 2017
Z-0728-2017Class IICarry bar which is an accessory to a lift used for patients in hospitals and other facilities. RecaAugust 30, 2016
Z-0285-2016Class IIPrism Medical P-300 Portable Consumer Lift; PN 303050, 303050R, and 303051; weight specification 300September 8, 2015
Z-0284-2016Class IIPrism Medical C-300 Consumer Ceiling Lift; PN 330050, 330050R, 330053, 330053R, and 330057; weight sSeptember 8, 2015
Z-2269-2015Class IIPrism Medical P-440 Portable Ceiling Lift; PN 303070 and 303070R (refurbished); Patient lift with weJune 24, 2015
Z-2270-2015Class IIPrism Medical P-600 Portable Ceiling Lift; PN 303090. Patient lift with weight specification of 600 June 24, 2015