Stryker Medical Division of Stryker Corporation recalls ProCuity bed series, model number 3009, item number: 3009PX-
Recalled Product
ProCuity bed series, model number 3009, item number: 3009PX-LEX-400.
Hazard / Issue
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: UDI-DI (GTIN): 07613327541229. Serial numbers: 2203001674, 2203001673, 2203001662, 2203001328, 2112001472, 2201001284, 2201001262, 2201001258, 2210002490 , 2210002246 , 2203001157 , 2210000264 , 2108002021 , 2207000782 , 2207000778 , 2208000442 , 2107000549 , 2103001807 , 2107000349 , 2206000057 , 2206000027 , 2206000007 , 2206000001 , 2105001397 , 2105001386 , 2202000874 , 2202000831 , 2203002026 , 2203001847 , 2105001777 , 2105001733 , 2105001730 , 2105001704 , 2105001694 , 2212001339, 2212001353, 2212001354, 2212001371 , 2209001039 , 2107000414 , 2104003152 , 2106002729 , 2106002525 , 2210002613 , 2210002592 , 2209001197 , 2212001462, 2209000157 , 2209000148 , 2209000132 , 2209000131 , 2209000129 , 2209000124 , 2208002626 , 2208002260 , 2208002189 , 2208002119 , 2208002117 , 2109001048 , 2102003094 , 2101002546 , 2101002504 , 2110000684 , 2203000449 , 2203000444 , 2202000882 , 2212000954 , 2212000966 , 2212000971 , 2212000987 , 2212000995 , 2212001051 , 2212001056 , 2212001072 , 2209001661 , 2212000653, 2212000632 , 2212000137 , 2212000053 , 2110001030 , 2202000968 , 2210002107 , 2210002092 , 2210002090 , 2102002723 , 2102002735 , 2210002089 , 2210002086 , 2210002064 , 2210001780 , 2102002782 , 2102001851 , 2210001325 , 2210001382 , 2210001395 , 2211000549 , 2211003332 , 2211000994 , 2211000932 , 2111001755 , 2111001751 , 2209000399 , 2206000124 , 2206000106 , 2104003071 , 2111000703 , 2111001128 , 2111000790 , 2111000789 , 2012000962 , 2011000951 , 2011000882 , 2109002087 , 2109002064 , 2109002045 , 2011002330 , 2112001153 , 2112001143
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