Stryker Communications recalls
Every recall we track for Stryker Communications — 11 in all, from 2018–2026 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
Recalls from Stryker Communications peaked in 2019 (4); 11 since 2017. 9% rated “stop using now”.
All FDA recall records for Stryker Communications 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 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 2 | 1 | 0 | 3 |
| 2019 | 1 | 3 | 0 | 0 | 4 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 1 | 0 | 0 | 1 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 1 | 0 | 0 | 1 |
| 2025 | 0 | 0 | 1 | 0 | 1 |
| 2026 (to date) | 0 | 1 | 0 | 0 | 1 |
What to do if you have a recalled Stryker Communications 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 Communications recalls
10 shown- Use cautionMedical device
Stryker Communications recalls Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001
Stryker recalls CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001 due to potential ceiling cover failure under weight. All units are affected.
StrykerFeb 23, 2026 - Lower riskMedical device
Stryker Communications recalls Chromophare Surgical Light System, REF: CH00000001; SLX to Oculan NFC Upgrade Kit, REF: P60034
Stryker recalls Chromophare Surgical Light Systems with stress lines in powder coating that may chip. Affected units include specific REF/serial numbers. No remedy stated in recall notice.
StrykerJul 15, 2025 - Use cautionMedical device
Stryker Communications recalls Chromophare Surgical Light System , REF CH00000001
Stryker recalls Chromophare Surgical Light Systems with insufficient mounting force causing stability issues. Affected units may tip over during surgery.
StrykerFeb 8, 2024 - Use cautionMedical device
Stryker Communications recalls S-Series Equipment Management System; Model Number(s):0682400550; UDI: 07613327400502 Components that are affected
Stryker recalls S-Series Equipment Management System models with capacitive touch controls that may disengage when electrocautery devices are used, posing a risk of equipment malfunction during medical procedures.
StrykerJan 29, 2021 - Stop using nowMedical device
Stryker Communications recalls Berchtold Chromophare Ceiling Mounted Surgical Light System, Catalog #CH13000000
Stryker recalls Berchtold Chromophare ceiling-mounted surgical lights with catalog #CH13000000 due to risk of falling, potentially causing serious injury to patients or healthcare providers.
StrykerOct 11, 2019 - Use cautionMedical device
Stryker Communications recalls Berchtold Chromophare Dual Monitor Carrier Arm or Dual Flat Panel, a component of Berchtold Chromophare Ceiling Mounted
Stryker recalls Berchtold Chromophare Dual Monitor Carrier Arms with serial numbers DFP-075-0307-0001 to DFP-075-1014-0230 due to potential insufficient welds in mounts.
StrykerAug 1, 2019 - Use cautionMedical device
Stryker Communications recalls Berchtold Chromophare F628 Surgical Lights. Product Usage: The medical lights are for usage in hospital treatment
Stryker recalls Berchtold Chromophare F628 surgical lights with serial numbers 83171-0017818 to 83171-0123938 due to risk of back cover detachment during use in hospitals.
Stryker CommunicationsMar 22, 2019 - Use cautionMedical device
Stryker Communications recalls EDS Light Suspension, Central Axis, a component of the Stryker Visum LED Surgical Lighting System, with the following
Stryker recalls EDS Light Suspension components for potential insufficient joint assembly, risking surgical lighting system failure during procedures. Affected units include specific catalog numbers and serial ranges.
StrykerNov 13, 2018 - Lower riskMedical device
Stryker Communications recalls Berchtold Chromophare Ceiling Mounted Surgical Light System, Catalog #CH13000000. Product Usage: Chromophare surgical
Stryker is a leading global manufacturer of medical devices and healthcare products. The company has a long history of innovation and quality in the healthcare industry.
StrykerJan 29, 2018 - Use cautionMedical device
Stryker Communications recalls Berchtold Chromophare Dual Monitor Carrier Arm or Dual Flat Panel, a component of Berchtold Chromophare Ceiling Mounted
Stryker recalls Berchtold Chromophare Dual Monitor Carrier Arms with possible insufficient welds. Affected units have specific serial numbers in the US and Canada. Stop using immediately to prevent potential failure.
StrykerJan 26, 2018
Stryker Communications recall questions
How many recalls has Stryker Communications had?
11 recalls from Stryker Communications are on record with U.S. safety agencies, from 2018–2026.
What is the most recent Stryker Communications recall?
Stryker Communications recalls Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001, dated Feb 23, 2026. Every Stryker Communications recall is listed on this page, newest first.
What should I do if I have a recalled Stryker Communications 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 Communications 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.