Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

ยฉ 2026 Go Backs. All rights reserved.

Medium RiskFDA Device
Medical Devices/Diagnostic Equipment

Sysmex TS-10/TS-10H Tube Sorters Recalled for Unexpected Lift Movement

Agency Publication Date: January 21, 2026
Share:
Sign in to monitor this recall

Summary

Sysmex America, Inc. is recalling 44 units of its TS-10 and TS-10H Tube Sorter systems, which are used in laboratories to automatically sort barcoded sample tubes. The recall affects systems with catalog number BN168792 running software versions 00-17. Under specific conditions, the lift's electromagnetic holding force can fail, causing the lift to move downward unexpectedly. Laboratories should stop using the recalled equipment and contact Sysmex America or their distributor to arrange for a return, replacement, or correction.

Risk

The lift mechanism may lose its holding force and drop suddenly, which could lead to physical injury for laboratory personnel or damage to clinical samples. No injuries or specific incidents were reported in the recall data.

What You Should Do

  1. This recall affects Sysmex TS-10 and TS-10H Tube Sorter systems with Catalog Number BN168792 running software versions 00-17.
  2. Affected serial numbers are printed on the device label. See the Affected Products section below for the full list of affected codes.
  3. Stop using the recalled sorting system immediately.
  4. Contact Sysmex America or your authorized distributor to arrange for a return, replacement, or mechanical correction of the sorter unit.
  5. Call the FDA at 1-888-463-6332 for more information regarding this medical device recall.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled product. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: TS-10/TS-10H Tube Sorter
Variants: Software versions 00-17
Model / REF:
BN168792
Serial Numbers:
11281
11611
11918
11790
12040
11991
12218
11950
11795
11533
11635
12054
11610
11453
11753
11539
11990
12298
11774
11541
11981
11788
11834
12005
11907
11524
12237
11246
12154
12104
12299
12176
11711
11420
12153
12177
12074
11405
11303
12039
11250
11336
12137
12075

Automatic sorting system for sorting barcoded sample tubes.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98213
Status: Active
Manufacturer: Sysmex America, Inc.
Sold By: Authorized Sysmex distributors
Manufactured In: United States
Units Affected: 44 units
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.