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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 93317

13 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
August 30, 2023
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Stryker Medical Division of Stryker Corporation

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

13 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 13

ProCuity bed series, model number 3009, item number: 300900000000,

Z-0424-2024
Recall number
Z-0424-2024
Initiated
August 30, 2023
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

Code information

UDI-DI (GTIN): 07613327512656. Serial numbers: 2207000698, 2207000676, 2207000619, 2206001100, 2206001090, 2206001089, 2206001086, 2206001084, 2208001745, 2208001734, 2208001725, 2208001724, 2208000397, 2208000394, 2208000032, 2209002157, 2209002158, 2209002165, 2210000711 , 2210000721 , 2210000723 , 2111000494 , 2206001248 , 2206001250 , 2206001265 , 2206001273 , 2206001317 , 2207000023 , 2207000078 , 2207000303 , 2207000307 , 2207000342 , 2207000350 , 2207000353 , 2207000358 , 2110002355 , 2108002264 , 2209000269 , 2106002756 , 2103001270 , 2109000898 , 2109001004 , 2108001784 , 2107001856 , 2208000874 , 2208000873 , 2208000814 , 2208000805 , 2104001582 , 2104003135 , 2104003758 , 2104003772 , 2104003778 , 2104003786 , 2104003798 , 2104004415 , 2104004431 , 2104004441 , 2104004491 , 2104004537 , 2104004993 , 2104004997 , 2104004998 , 2104005012 , 2104005013 , 2105000649 , 2105000657 , 2105001594 , 2105001621 , 2107000100 , 2107000102 , 2208000795 , 2108000833 , 2211004443, 2211004441, 2211004293, 2211004095 , 2211004050 , 2211003541 , 2209002035 , 2205000370 , 2208001249 , 2208001250 , 2202001692 , 2108002072 , 2108002161 , 2202001958 , 2202002003 , 2205000361 , 2109001797 , 2208001175 , 2208001162 , 2208001044 , 2107001827 , 2208000995 , 2208000992 , 2208000980 , 2208000910 , 2208000854 , 2201001114 , 2208001148 , 2208001129 , 2207001981 , 2106001072 , 2206001367 , 2209002143 , 2208000569 , 2208000568 , 2208000507 , 2208000473 , 2109002479 , 2210002762 , 2112002175 , 2112001663 , 2112000049 , 2106002744 , 2109003074 , 2110000077 , 2110000082 , 2105000094 , 2105004609 , 2108000595 , 2104000805 , 2108001834 , 2108001836 , 2208000577 , 2208000496 , 2201000319 , 2203002461 , 2108002656 , 2203001282 , 2109001070 , 2209002133 , 2112002188 , 2112001020 , 2211000729 , 2109002517 , 2103003835 , 2104000245 , 2207001763 , 2107000933 , 2102000258 , 2110000967 , 2110000965 , 2103000446 , 2108002753 , 2108002726 , 2108002685 , 2108002683 , 2108002673 , 2108002556 , 2108002533 , 2108002507 , 2105002810 , 2112000853 , 2105002764 , 2107000759 , 2209000686 , 2108001946 , 2108001932 , 2112001628 , 2111000528 , 2110001582 , 2111000399 , 2111000286 , 2111000092 , 2111001950 , 2110002881 , 2110002369 , 2207000860 , 2207000862 , 2109002846 , 2110002291 , 2110001555 , 2110001362 , 2108002306 , 2201000283 , 2108001939 , 2107001826 , 2210000028 , 2210000004 , 2111000392 , 2110002880 , 2110002867 , 2110000448 , 2110000458 , 2110002828 , 2110002819 , 2110002405 , 2110002399 , 2110001809 , 2101002085 , 2109002376 , 2110001384 , 2110002668 , 2111000409 , 2111000533 , 2112000343 , 2112000347 , 2109002824 , 2209002123 , 2208000334 , 2208000331 , 2107000836 , 2212000241 , 2212000236, 2212000223, 2212000217 , 2212000215 , 2208000075 , 2201000857 , 2108001491 , 2108001490 , 2108000825 , 2009000613 , 2106001220 , 2106001200 , 2106001197 , 2104001603 , 2201000196 , 2208001930 , 2208001924 , 2208001886 , 2210002945 , 2208001860 , 2111000090 , 2107001825 , 2109002592 , 2107000127 , 2107000115 , 2105002209 , 2205000426 , 2107001697 , 2202001129 , 2105002197 , 2105002192

Distribution pattern

Distribution US Nationwide including Puerto Rico, Australia, Canada, Chile, China, Mexico, Poland, Spain and Switzerland.

device · product 2 of 13

ProCuity bed series, model number 3009, item number: 3009PX-L-100.

Z-0425-2024
Recall number
Z-0425-2024
Initiated
August 30, 2023
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

Code information

UDI-DI (GTIN): 07613327541168. Serial numbers: 2111000766 & 2107000368

Distribution pattern

Distribution US Nationwide including Puerto Rico, Australia, Canada, Chile, China, Mexico, Poland, Spain and Switzerland.

device · product 3 of 13

ProCuity bed series, model number 3009, item number: 3009PX-L-200

Z-0426-2024
Recall number
Z-0426-2024
Initiated
August 30, 2023
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

Code information

UDI-DI (GTIN): 07613327541199 Serial numbers: 2211000305 , 2112000828 , 2109001676 , 2109001666 , 2209002657 , 2208001565 , 2208001555 , 2208001541 , 2203002178 , 2203002161 , 2203002159 , 2203002157 , 2106000232 , 2106000210

Distribution pattern

Distribution US Nationwide including Puerto Rico, Australia, Canada, Chile, China, Mexico, Poland, Spain and Switzerland.

device · product 4 of 13

ProCuity bed series, model number 3009, item number: 3009PX-LE-400.

Z-0427-2024
Recall number
Z-0427-2024
Initiated
August 30, 2023
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

Code information

UDI-DI (GTIN): 07613327541182. Serial numbers: 2105002838 , 2105002832 , 2202000312 , 2202000286 , 2202000278 , 2202000180 , 2106002241 , 2106001240 , 2107001002 , 2203001053 , 2203001898 , 2112001135 , 2211002054 , 2105002782 , 2210002902 , 2210002890 , 2210002876 , 2210002858 , 2210002848 , 2111001420 , 2206001182

Distribution pattern

Distribution US Nationwide including Puerto Rico, Australia, Canada, Chile, China, Mexico, Poland, Spain and Switzerland.

device · product 5 of 13

ProCuity bed series, model number 3009, item number: 3009PX-LE-450.

Z-0428-2024
Recall number
Z-0428-2024
Initiated
August 30, 2023
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

Code information

UDI-DI (GTIN): 07613327541175. Serial numbers: 2109000993 , 2208000147 , 2209000850 , 2211002051 , 2202000910 , 2209000408 , 2205000619 , 2205000615 , 2205000612 , 2205000587 , 2205000746 , 2205000745 , 2205000739 , 2109000135 , 2109000124

Distribution pattern

Distribution US Nationwide including Puerto Rico, Australia, Canada, Chile, China, Mexico, Poland, Spain and Switzerland.

device · product 6 of 13

ProCuity bed series, model number 3009, item number: 3009PX-LEX-400.

Z-0429-2024
Recall number
Z-0429-2024
Initiated
August 30, 2023
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

Code information

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

Distribution pattern

Distribution US Nationwide including Puerto Rico, Australia, Canada, Chile, China, Mexico, Poland, Spain and Switzerland.

device · product 7 of 13

ProCuity bed series, model number 3009, item number: 3009PX-LEX-450.

Z-0430-2024
Recall number
Z-0430-2024
Initiated
August 30, 2023
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

Code information

UDI-DI (GTIN): 07613327541236. Serial numbers: 2207000806 , 2101001244 , 2206000635 , 2206000628 , 2206000626 , 2206000483 , 2206000479 , 2206000412 , 2206000405 , 2206000401 , 2206000177 , 2205000560 , 2107001062 , 2107001046 , 2205000843 , 2205000841 , 2205000840 , 2205000836 , 2205000832 , 2208000197 , 2208000174 , 2208000156 , 2211002859 , 2205000935 , 2207001318 , 2207001289 , 2207001178 , 2207001163 , 2207001155 , 2207001114 , 2211000184 , 2211000209 , 2207001100 , 2207001097 , 2207001095 , 2207001600 , 2207001071 , 2207001037 , 2207001028 , 2204000753 , 2204000750 , 2204000542 , 2204000195 , 2203002255 , 2203002137 , 2203002129 , 2203001533 , 2203001527 , 2203001424 , 2203001163 , 2203000232 , 2203000230 , 2203000208 , 2203000044 , 2203000036 , 2203000033 , 2107001094 , 2203000005 , 2202001013 , 2202000678 , 2202000506 , 2104002546 , 2104002532 , 2104002512 , 2104002501 , 2104001704 , 2105005200 , 2103001843 , 2103001783 , 2102000290 , 2210003278 , 2208000758 , 2109002018 , 2011000511 , 2011000497 , 2202000089 , 2211004212 , 2109002745

Distribution pattern

Distribution US Nationwide including Puerto Rico, Australia, Canada, Chile, China, Mexico, Poland, Spain and Switzerland.

device · product 8 of 13

ProCuity bed series, model number 3009, item number: 3009PX-Z-450.

Z-0431-2024
Recall number
Z-0431-2024
Initiated
August 30, 2023
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

Code information

UDI-DI (GTIN): 07613327541250. Serial number: 2110001715

Distribution pattern

Distribution US Nationwide including Puerto Rico, Australia, Canada, Chile, China, Mexico, Poland, Spain and Switzerland.

device · product 9 of 13

ProCuity bed series, model number 3009, item number: 3009PX-ZM-450.

Z-0432-2024
Recall number
Z-0432-2024
Initiated
August 30, 2023
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

Code information

UDI-DI (GTIN): 07613327541274 . Serial numbers: 2208002548 & 2212001984

Distribution pattern

Distribution US Nationwide including Puerto Rico, Australia, Canada, Chile, China, Mexico, Poland, Spain and Switzerland.

device · product 10 of 13

ProCuity bed series, model number 3009, item number: 3009PX-ZM-600.

Z-0433-2024
Recall number
Z-0433-2024
Initiated
August 30, 2023
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

Code information

UDI-DI (GTIN): 07613327541311. Serial numbers: 2201000173, 2110001895, 2203001506, 2110000413, 2110000411, 2208002037, 2208002030, 2208002019& 2212000691

Distribution pattern

Distribution US Nationwide including Puerto Rico, Australia, Canada, Chile, China, Mexico, Poland, Spain and Switzerland.

device · product 11 of 13

ProCurity bed series, model number 3009, item number: 3009PX-ZMX-450.

Z-0434-2024
Recall number
Z-0434-2024
Initiated
August 30, 2023
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

Code information

UDI-DI (GTIN): 07613327541304 . Serial number: 2212000205

Distribution pattern

Distribution US Nationwide including Puerto Rico, Australia, Canada, Chile, China, Mexico, Poland, Spain and Switzerland.

device · product 12 of 13

ProCurity bed series, model number 3009, item number: 3009PX-ZMX-600.

Z-0435-2024
Recall number
Z-0435-2024
Initiated
August 30, 2023
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

Code information

UDI-DI (GTIN): 07613327541328. Serial numbers: 2209001834, 2209001941 , 2209001939 , 2211002329 , 2211002319 , 2211000556 , 2205000776 , 2106000019 , 2202002062 , 2106001528 , 2106001515 , 2209001539 , 2203000249 , 2106002482 , 2202001091 , 2203000298 , 2203000098 , 2108000232 , 2208000679 , 2110000200 , 2106002061 , 2106002051 , 2106001697 , 2211004469 , 2211004828 , 2206001229 , 2206001234 , 2211004824 , 2106001589 , 2209002761 , 2209002730 , 2209002674 , 2111000113 , 2111000111 , 2208001113

Distribution pattern

Distribution US Nationwide including Puerto Rico, Australia, Canada, Chile, China, Mexico, Poland, Spain and Switzerland.

device · product 13 of 13

ProCurity bed series, model number 3009, item number: 3009PX-ZX-450.

Z-0436-2024
Recall number
Z-0436-2024
Initiated
August 30, 2023
Classification
Class II
Status
Ongoing
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

Code information

UDI-DI (GTIN): 07613327541366. Serial numbers: 2105004433, 2105004422, 2110001418, 2110001260, 2110000511, & 2110000496

Distribution pattern

Distribution US Nationwide including Puerto Rico, Australia, Canada, Chile, China, Mexico, Poland, Spain and Switzerland.