Z-0277-2010

Stryker Medical transport stretcher, Stryker Medical, Portage, MI; Model 734. Wheeled hospital stretcher

Name: Z-0277-2010 Stryker Medical transport stretcher, Stryker Medical, Portage, MI; Model 734. Wheeled hospital stretcher
Creator: Stryker Medical Div. of Stryker Corporation
Published: 2009-08-10
License: https://open.fda.gov/license/

Stryker Medical / initiated 2009-08-10 / Terminated / root cause: manufacturing process

FDA source

Stryker Medical Div. of Stryker Corporation began a recall of Stryker Medical transport stretcher, Stryker Medical, Portage, MI; Model 734. Wheeled hospital stretcher on 2009-08-10. The reason FDA records is "The brake/steer pedal may seize, resulting in the brakes not working". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as manufacturing process.

Recall record

Recall number: Z-0277-2010
Status: Terminated
Initiated: 2009-08-10
Posted: 2009-11-17
Terminated: 2010-10-29
Recalling firm: Stryker Medical
Product: Stryker Medical transport stretcher, Stryker Medical, Portage, MI; Model 734. Wheeled hospital stretcher.
Product code: FPO Stretcher, Wheeled
Reason for recall: The brake/steer pedal may seize, resulting in the brakes not working.
Root cause tag: manufacturing process
FDA root cause: Nonconforming Material/Component
Action: Consignees were notified by letter dated August 10, 2009 that Stryker will contact them to upgrade the stretchers within 6 months. The recall was expanded in scope to include additional serial numbers by a second letter dated September 17, 2009, which was issued to additional consignees who had not been previously notified of the recall, as well as the consignees who had been issued the August 10, 2009 letter.
Quantity in commerce: 241
Distribution: Nationwide, Argentina, Australia, Brazil, Canada, Chile, China, France, Germany, Greece, India, Italy, Japan, Korea, Latin America, Malaysia, Mexico, Netherlands, Philippines, Poland, Portugal, Singapore, South Africa, Spain, Switzerland, Taiwan, and United Kingdom,
Product codes and lots: Serial numbers 0804103191, 0804103192, 0804103193, 0804103194, 0804103195, 0804103196, 0804103197, 0804103198, 0804103199, 0804103200, 0804103201, 0804103202, 0804103203, 0804104321, 0804104322, 0804104323, 0804104324, 0804104325, 0804104326, 0804104374, 0804105901, 0804105902, 0804105903, 0804105904, 0804105905, 0804105906, 0804105907, 0804105908, 0804105909, 0804105910, 0804105911, 0804105912, 0804105913, 0804105914, 0804105915, 0805099507, 0805099508, 0805099509, 0805101711, 0805101712, 0805101713, 0805101714, 0805101715, 0805101716, 0805101717, 0805101718, 0805101719, 0805101720, 0805101721, 0805101722, 0805101723, 0805101724, 0805101981, 0805101982, 0805101983, 0805101984, 0805101985, 0805101986, 0805101987, 0805101988, 0805101989, 0805101990, 0805101991, 0805101992, 0805101993, 0805101994, 0805101995, 0805101996, 0805101997, 0805101998, 0805101999, 0806099631, 0806099632, 0806099633, 0806099634, 0806099635, 0806099636, 0806099637, 0806099638, 0806099639, 0806099640, 0806099641, 0806099642, 0806099643, 0806099644, 0806099645, 0806099698, 0806099699, 0806099700, 0806101641, 0806101642, 0806101643, 0806101644, 0806101645, 0806101646, 0806101647, 0806101713, 0806101714, 0806101715, 0806101716, 0806101717, 0807103688, 0807103689, 0807103731, 0807103732, 0807103733, 0807103734, 0807103735, 0807103736, 0807103737, 0807103738, 0807103739, 0807103740, 0807103741, 0807103742, 0807103743, 0807103744, 0807103745, 0807108409, 0808100984, 0808100985, 0808100986, 0808100987, 0808100988, 0808105151, 0808105152, 0808105153, 0808105154, 0808105155, 0808105156, 0808105157, 0808105158, 0808105159, 0808105160, 0808105161, 0808105162, 0808105163, 0808105164, 0808105165, 0808105166, 0808105167, 0808105168, 0808106551, 0808106552, 0808106553, 0808106554, 0808106555, 0808106556, 0808106557, 0808106558, 0808106559, 0808106560, 0808106561, 0808106562, 0808106563, 0808106564, 0808106565, 0808106571, 0808106572, 0808106573, 0808106574, 0808106575, 0808106576, 0808106577, 0808106578, 0808106579, 0808106580, 0810105201, 0810105202, 0810105203, 0811101373, 0812102621, 0812102622, 0812102623, 0812102624, 0812102625, 0812102626, 0812102627, 0812102628, 0812102629, 0812102630, 0812102731, 0812102732, 0812102733, 0812102734, 0812102735, 0812102736, 0812102737, 0812102738, 0901032081, 0901032082, 0901032083, 0901032084, 0901032085, 0901032086, 0901032087, 0901032088, 0901032981, 0901032982, 0901032983, 0901032984, 0901032985, 0901032986, 0901032987, 0901032988, 0901032989, 0901032990, 0901032991, 0901032992, 0901032993, 0901032994, 0901032995, 0902030031, 0902030032, 0902030033, 0902030034, 0902030035, 0902030036, 0902030371, 0902030372, 0902030373, 0902030374, 0902030375, 0902030376, 0902030377, 0902030378, 0902030379, 0902030380, 0902032821, 0902032822, 0902032823, 0902032824, 0902032825, 0902032826, 0902032827, 0902032828, 0902032829, 0903034667, 0903034668, 0903034669 and 0903034670.

Product code FPO

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-10-07, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)