Stryker Medical Division of Stryker Corporation recalls
Every recall we track for Stryker Medical Division of Stryker Corporation — 51 in all, from 2017–2026 — plus the complaints and injury reports the public filed about them. 2 are rated “stop using now”.
Recalls per year, by danger level
Recalls from Stryker Medical Division of Stryker Corporation peaked in 2021 (19); 51 since 2017. 4% rated “stop using now”.
All FDA recall records for Stryker Medical Division of Stryker Corporation since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 1 | 1 | 0 | 2 |
| 2018 | 1 | 5 | 3 | 0 | 9 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 2 | 0 | 0 | 2 |
| 2021 | 0 | 19 | 0 | 0 | 19 |
| 2022 | 0 | 1 | 0 | 0 | 1 |
| 2023 | 1 | 14 | 0 | 0 | 15 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 2 | 0 | 2 |
| 2026 (to date) | 0 | 0 | 1 | 0 | 1 |
What to do if you have a recalled Stryker Medical Division of Stryker Corporation product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Stryker Medical Division of Stryker Corporation recalls
18 shown- Lower riskMedical device
Stryker Medical Division of Stryker Corporation recalls Cub Pediatric Crib, Model FL19H
Stryker recalls Cub Pediatric Crib Model FL19H in the USA for missing two access door warning labels. This could lead to safety risks if the labels are needed for proper use.
StrykerFeb 18, 2026 - Lower riskMedical device
Stryker Medical Division of Stryker Corporation recalls Stryker Arise 1000EX mattress, Part Number 2236000000
Stryker recalls certain Arise 1000EX mattresses (Part Number 2236000000) sold near MV3 beds due to untested compatibility. These products are not designed to be used together.
StrykerOct 31, 2025 - Use cautionMedical device
Stryker Medical Division of Stryker Corporation recalls ProCuity bed series, model number 3009, item number: 3009PX-LE-400.
Stryker recalls ProCuity bed model 3009 with missing electrical safety test values, risking tissue burns or electrical shock. Affected units have specific serial numbers and item numbers.
StrykerAug 30, 2023 - Use cautionMedical device
Stryker Medical Division of Stryker Corporation recalls Power-PRO 2- A powered ambulance cot that consists of a platform, including a mattress, mounted on a wheeled,
Stryker recalls Power-PRO 2 ambulance cots with serial numbers from 2112001485 to 2211001651. The base leg assembly may bend, causing difficulty engaging/disengaging from fasteners and affecting loading/unloading from ambulances. Affected units shipped between February 2022 and February 2023.
StrykerMay 24, 2023 - Use cautionMedical device
Stryker Medical Division of Stryker Corporation recalls Power-PRO 2 . Intended as an ambulance cot to transport a patient to or from an emergency or non-emergency location.
Stryker recalls Power-PRO 2 ambulance cots with insufficient epoxy causing head or foot sections to detach during transport. Affected units have specific serial numbers. Contact Stryker for repair or replacement.
StrykerFeb 1, 2023 - Use cautionMedical device
Stryker Medical Division of Stryker Corporation recalls Power-PRO 2, Model No. 6507, Item No. 650705550001 (US); 650700000000 (International)
Stryker recalls Power-PRO 2 cots with model 6507 that may move unexpectedly due to damaged cables, risking soft tissue injuries like scrapes or bruises to patients.
StrykerNov 11, 2022 - Use cautionMedical device
Stryker Medical Division of Stryker Corporation recalls Prime Fifth Wheel Stretcher-stretcher may be used for minor procedures and short-term stay (treatment and recovery,
Stryker recalls Prime Fifth Wheel Stretcher model 1105 for home use. The device is intended for healthcare facilities but may be used at home without proper training, risking injury.
StrykerMay 12, 2021 - Use cautionMedical device
Stryker Medical Division of Stryker Corporation recalls Stryker IsoAir 2.0 support surface-provides pressure redistribution and is intended to assist in management of the
Stryker recalls IsoAir 2.0 support surfaces with potential CPR connector removal issues during cardiac arrest. Affected units have specific serial numbers and model 2941-001-100. Contact Stryker for details.
StrykerAug 12, 2020 - Use cautionMedical device
Stryker Medical Division of Stryker Corporation recalls Stryker Power-PRO TL cot-powered ambulance cot Model Number 6550 - Product Usage: is a powered wheeled stretcher that
Stryker recalls Power-PRO TL ambulance cots (model 6550) that may not meet crash test standard BS EN 1789. Affected units include specific serial numbers listed in the recall notice.
StrykerApr 7, 2020 - Use cautionMedical device
Stryker Medical Division of Stryker Corporation recalls Power-LOAD Cot Fastening System, Model #6390, Catalog #6390-000-000
Stryker recalls Power-LOAD Cot Fastening System Model 6390 (Catalog #6390-000-000) due to risk of broken floor plates during ambulance patient transport. Affected units have serial numbers listed in the recall notice.
StrykerNov 20, 2018 - Lower riskMedical device
Stryker Medical Division of Stryker Corporation recalls Naera Hospital Bassinet, Model No. 4402
Stryker is a global leader in medical technology, providing innovative solutions for healthcare professionals and patients worldwide.
StrykerOct 10, 2018 - Use cautionMedical device
Stryker Medical Division of Stryker Corporation recalls The Spirit Plus Bed, Model 5600 Spirit Plus /with high rail siderail option
Stryker recalls Spirit Plus Bed Model 5600 with high rail siderail option due to potential entrapment risk. Affected units have specific serial numbers listed in the recall notice.
StrykerOct 8, 2018 - Use cautionMedical device
Stryker Medical Division of Stryker Corporation recalls Altrix¿ Precision Temperature Management System Model: 8001Product Usage: The Altrix system is intended for circulating
Stryker recalls Altrix Model 8001 units made between Oct 2016 and June 2017 due to potential alarm fatigue and device faults that could affect patient temperature monitoring.
StrykerSep 6, 2018 - Use cautionMedical device
Stryker Medical Division of Stryker Corporation recalls IsoFlex LAL Support Surface, Model Number 2860 Product Usage: : The IsoFlex LAL support surface assists in the
Stryker recalls 2860 IsoFlex LAL Support Surfaces with non-conforming fire barrier. These medical devices for pressure injury prevention may pose fire risk if improperly used in healthcare settings.
StrykerAug 13, 2018 - Stop using nowMedical device
Stryker Medical Division of Stryker Corporation recalls Power-LOAD Cot Fastening System, Model #6390, Catalog #6390-000-000, UDI: 07613327261523 Power-LOAD is intended to
Stryker recalls Power-LOAD Cot Fastening System Model #6390 due to risk of broken floor plates during ambulance transport. Affected units have specific serial numbers. Stop using immediately to prevent potential injury.
StrykerMar 12, 2018 - Lower riskMedical device
Stryker Medical Division of Stryker Corporation recalls 6381 M-1 Cot Fastener, catalog no. 6381000000
Stryker recalls 6381 M-1 Cot Fasteners with missing safety warnings in manuals. Owners should check serial numbers 170740538-170740540 for affected units.
StrykerMar 9, 2018 - Lower riskMedical device
Stryker Medical Division of Stryker Corporation recalls T/Pump temperature therapy pump, Models TP700 and TP700C
Stryker recalls T/Pump temperature therapy pumps (models TP700 and TP700C) due to incorrect manual updates adding 'heat conservation for normothermia maintenance' to indications. No immediate action needed as the hazard is a documentation error.
StrykerNov 7, 2017 - Use cautionMedical device
Stryker Medical Division of Stryker Corporation recalls MA3320-PM Premium Adult - SYK Mistral-Air Premium Blankets. MODEL #: MA3302-PM. CATALOG #(s): MA3302-PM
Stryker recalls Mistral-Air Premium Blankets (model MA3302-PM) that may conduct electricity during high-energy defibrillation, risking electrical shock. Affected units include specific lots.
StrykerJul 21, 2017
Stryker Medical Division of Stryker Corporation recall questions
How many recalls has Stryker Medical Division of Stryker Corporation had?
51 recalls from Stryker Medical Division of Stryker Corporation are on record with U.S. safety agencies, from 2017–2026.
What is the most recent Stryker Medical Division of Stryker Corporation recall?
Stryker Medical Division of Stryker Corporation recalls Cub Pediatric Crib, Model FL19H, dated Feb 18, 2026. Every Stryker Medical Division of Stryker Corporation recall is listed on this page, newest first.
What should I do if I have a recalled Stryker Medical Division of Stryker Corporation product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Stryker Medical Division of Stryker Corporation recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.