Recall archive / FDA device enforcement
ProCuity bed series, model number 3009, item number: 3009PX-LEX-400. — FDA record Z-0429-2024
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Aug 30, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- ProCuity bed series, model number 3009, item number: 3009PX-LEX-400.
- Reason
- Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
- Classification
- Class II
- Recalling firm
- Stryker Medical Division of Stryker Corporation
- Quantity
- Not supplied
- Agency-reported status
- Ongoing
- Source record identifier
- Z-0429-2024
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | 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 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Distribution US Nationwide including Puerto Rico, Australia, Canada, Chile, China, Mexico, Poland, Spain and Switzerland.
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
- Alaska
- Alabama
- Arkansas
- Arizona
- California
- Colorado
- Connecticut
- Delaware
- Florida
- Georgia
- Hawaii
- Iowa
- Idaho
- Illinois
- Indiana
- Kansas
- Kentucky
- Louisiana
- Massachusetts
- Maryland
- Maine
- Michigan
- Minnesota
- Missouri
- Mississippi
- Montana
- North Carolina
- North Dakota
- Nebraska
- New Hampshire
- New Jersey
- New Mexico
- Nevada
- New York
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- Rhode Island
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Virginia
- Vermont
- Washington
- Wisconsin
- West Virginia
- Wyoming
Dates in the source
- Report date
- Dec 13, 2023
- Recall initiation date
- Aug 30, 2023
- Center classification date
- Dec 1, 2023
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.