Beckman Coulter Power Processor 3K Stockyard Module: Missing Splash Guard Risk
Beckman Coulter recalls Power Processor 3K Stockyard modules with missing splash guards that could expose users to hazardous materials. Affected units have specific serial numbers and catalog codes.
Use caution until it’s fixed
Missing splash guard which may expose users to hazardous materials. .
Contact the company
What happened, in plain English
Beckman Coulter is recalling Power Processor 3K Stockyard refrigerated modules because they may lack a splash guard, potentially exposing users to hazardous materials. This is a safety issue that requires attention to prevent exposure risks. Read more at govinfonow.com/recall/62136-beckman-coulter-power-processor-3k-stockyard-module-missing-splash-guard.
Source Summary by GovInfoNow · govinfonow.com/recall/62136-beckman-coulter-power-processor-3k-stockyard-module-missing-splash-guard · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0117-2022
Cite this page
“Beckman Coulter Power Processor 3K Stockyard Module: Missing Splash Guard Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/62136-beckman-coulter-power-processor-3k-stockyard-module-missing-splash-guard. Based on FDA recall #Z-0117-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0117-2022%22&limit=1).
Why it’s dangerous
The missing splash guard can allow hazardous materials to splash onto users, increasing the risk of exposure to harmful substances. This is especially concerning in environments where the equipment is used with chemicals or other hazardous materials.
Who’s affected
Users of the Power Processor 3K Stockyard refrigerated modules are affected, particularly those handling the equipment in laboratory or industrial settings where hazardous materials are used. Individuals with the specific serial numbers listed in the recall are most at risk.
How to tell if you have this one
Check if your Power Processor 3K Stockyard refrigerated module has a serial number listed in the recall (e.g., 90HF1304006, 90AM0805001, etc.) or catalog number A88116 or 6915556. The recall covers specific models sold with these identifiers.
- Brand
Beckman Coulter- Category
Medical device
What to do — step by step
Check for Missing Splash Guard
Inspect your Power Processor 3K Stockyard module for a splash guard; if missing, stop using it immediately.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 21 states.
FDA distribution: “U.S. Nationwide Distribution in the states of: CA, GA, IA, ID, IL, IN, LA, MA, MI, MS, NJ, NY, OH, OR, PA, SC, SD, TN, TX, WA, and WV O.U.S.: Canada, China, Spain, France, United Kingdom, Israel, Italy, South Korea, Kuwait, Lebanon,…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: California, Georgia, Idaho, Illinois, Indiana, Iowa, Louisiana, Massachusetts, Michigan, Mississippi, New Jersey, New York, Ohio, Oregon, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Washington, West Virginia.
Recall timeline
FDA published this recall 3 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
Similar recalls
Latest medical device recalls
Keep exploring
Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-0117-2022 (July 28, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0117-2022 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.