CLASS II ONGOING Device recall · Reported 4 Dec 2024 · FDA Enforcement Report

Autosampler, Models: Sil-20ACXR CL, Sil-20ACHT CL, Sil-30AC CL recalled

Shimadzu Corp. Analytical & Measuring Instruments Div is recalling Autosampler, Models: Sil-20ACXR CL, Sil-20ACHT CL, Sil-30AC CL, distributed nationwide in the US. The recall was initiated on 9 Oct 2024 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesModel/UDI-DI/Serial Number: SIL-20ACXR CL/04540217420131/L20995250001, L20995250002, L20995250003, L20995250004, L20995250005, L20995250006, L20995250007, L20995250008, L20995350010, L20995350011, L20995350012, L20995350013, L20995350014, L20995350015, L20995450016, L20995450017, L20995450018, L20995450019, L20995450020, L20995450021, L20995450022, L20995450023, L20995450024, L20995450025, L20995450026, L20995550027, L20995550028, L20995550029, L20995550030, L20995650031, L20995650032, L20995650033, L20995650034, L20995650035, L20995650036, L20995650037, L20995650038, L20995650039, L20995650040, L20995650041, L20995650042, L20995650043, L20995650044, L20995650045, L20995650046, L20995560001, L20995660002, L20995660003, L20995660004, L20995660005, L20995660006, L20995660007, L20995660008, L20995660009, L20995660010, L20995660011, L20995660012, L20995660013, L20995660014, L20995660015, L20995660016, L20995660017, L20995660018, L20995660019, L20995660020, L20995660021, L20995660022, L20995660023, L20995660024, L20995660025, L20995660026, L20995660027, L20995660028, L20995660029, L20995660030, L20995660031, L20995660032, L20995660033, L20995660034, L20995660035, L20995660036, L20995660037, L20995660038, L20995660039, L20995660040, L20995660041, L20995660042, L20995660043, L20995660044, L20995660045, L20995660046, L20995660047, L20995660048, L20995660049, L20995660050, L20995660051, L20995660052, L20995660053, L20995660054, L20995660055, L20995660056, L20995660057, L20995250009, L20995270001, L20995270002, L20995270003, L20995270004, L20995270005, L20995370006, L20995370007, L20995370008, L20995370009, L20995370010, L20995370011, L20995370012, L20995370013, L20995370014, L20995370015, L20995370016, L20995370017, L20995370018, L20995370019, L20995370020, L20995370021, L20995370022, L20995370023, L20995370024, L20995370025, L20995470028, L20995770032. SIL-20ACHT CL/04540217420124/L20985350001, L20985450002, L20985750003, L20985750004. SIL-30AC CL/04540217420155/L21005250001, L21005250002, L21005250003, L21005250004, L21005250005, L21005250006, L21005250007, L21005350008, L21005350009, L21005350010, L21005350011, L21005350012, L21005350013, L21005350014, L21005350015, L21005350016, L21005350017, L21005350018, L21005350019, L21005350020, L21005350021, L21005350022, L21005350023, L21005350024, L21005450025, L21005550026, L21005550027, L21005650028, L21005650029, L21005750030, L21005750031, L21005570001, L21005570002, L21005670003, L21005670004, L21005670005, L21005670006, L21005670007, L21005670008, L21005770009, L21005770010, L21005770011, L21005770012, L21005770013, L21005770014.

Quantity recalled179

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-0553-2025
FDA event ID: 95632
Recalling firm: Shimadzu Corp. Analytical & Measuring Instruments Div, Kyoto
Classification: Class II
Status: Ongoing
Recall initiated: 9 Oct 2024
FDA classified: 26 Nov 2024
Reported: 4 Dec 2024
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Packaging Defects
Device type: Other Medical Devices

Timeline

9 Oct 2024	Recall initiated by company
26 Nov 2024	Classified by FDA	+48 days
4 Dec 2024	Published in enforcement report	+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

There have been cases of failure of the main board due to condensation water drained from the Peltier dehumidifier, leaked out from the tray, resulting in a short circuit. In the serious case, the main board and adjacent cables are partly charred. In the minor case, the Y motor and its surrounding die cast part become rusty. These failures could result in delay in patient sample testing.

Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.

Product as listed by the FDA

Autosampler, Models: SIL-20ACXR CL, SIL-20ACHT CL, SIL-30AC CL

Where it was distributed

Worldwide - US Nationwide distribution in the states of MS, AR, TX, CA, MA, MI, FL, OK, WI, IN, MN, OH, NJ, NY, IL, KY, NV, HI, SD, ID, MI, UT, WA, MO, VA, GA and the countries of DE, CN, JP, UY.

Nationwide Arkansas California Florida Georgia Hawaii Idaho Illinois Indiana Kentucky Massachusetts Michigan Minnesota Missouri Mississippi New Jersey Nevada New York Ohio Oklahoma South Dakota

Questions about this recall

Is Autosampler, Models: Sil-20ACXR CL, Sil-20ACHT CL, Sil-30AC CL recalled?

Yes. Shimadzu Corp. Analytical & Measuring Instruments Div recalled Autosampler, Models: Sil-20ACXR CL, Sil-20ACHT CL, Sil-30AC CL on 9 Oct 2024. The recall is Class II and its status is Ongoing. Recall number Z-0553-2025.

Why was it recalled?

Which lots are affected?

Model/UDI-DI/Serial Number: SIL-20ACXR CL/04540217420131/L20995250001, L20995250002, L20995250003, L20995250004, L20995250005, L20995250006, L20995250007, L20995250008, L20995350010, L20995350011, L20995350012, L20995350013, L20995350014, L20995350015, L20995450016, L20995450017, L20995450018, L20995450019, L20995450020, L20995450021, L20995450022, L20995450023, L20995450024, L20995450025, L20995450026, L20995550027, L20995550028, L20995550029, L20995550030, L20995650031, L20995650032, L20995650033, L20995650034, L20995650035, L20995650036, L20995650037, L20995650038, L20995650039, L20995650040, L20995650041, L20995650042, L20995650043, L20995650044, L20995650045, L20995650046, L20995560001, L20995660002, L20995660003, L20995660004, L20995660005, L20995660006, L20995660007, L20995660008, L20995660009, L20995660010, L20995660011, L20995660012, L20995660013, L20995660014, L20995660015, L20995660016, L20995660017, L20995660018, L20995660019, L20995660020, L20995660021, L20995660022, L20995660023, L20995660024, L20995660025, L20995660026, L20995660027, L20995660028, L20995660029, L20995660030, L20995660031, L20995660032, L20995660033, L20995660034, L20995660035, L20995660036, L20995660037, L20995660038, L20995660039, L20995660040, L20995660041, L20995660042, L20995660043, L20995660044, L20995660045, L20995660046, L20995660047, L20995660048, L20995660049, L20995660050, L20995660051, L20995660052, L20995660053, L20995660054, L20995660055, L20995660056, L20995660057, L20995250009, L20995270001, L20995270002, L20995270003, L20995270004, L20995270005, L20995370006, L20995370007, L20995370008, L20995370009, L20995370010, L20995370011, L20995370012, L20995370013, L20995370014, L20995370015, L20995370016, L20995370017, L20995370018, L20995370019, L20995370020, L20995370021, L20995370022, L20995370023, L20995370024, L20995370025, L20995470028, L20995770032. SIL-20ACHT CL/04540217420124/L20985350001, L20985450002, L20985750003, L20985750004. SIL-30AC CL/04540217420155/L21005250001, L21005250002, L21005250003, L21005250004, L21005250005, L21005250006, L21005250007, L21005350008, L21005350009, L21005350010, L21005350011, L21005350012, L21005350013, L21005350014, L21005350015, L21005350016, L21005350017, L21005350018, L21005350019, L21005350020, L21005350021, L21005350022, L21005350023, L21005350024, L21005450025, L21005550026, L21005550027, L21005650028, L21005650029, L21005750030, L21005750031, L21005570001, L21005570002, L21005670003, L21005670004, L21005670005, L21005670006, L21005670007, L21005670008, L21005770009, L21005770010, L21005770011, L21005770012, L21005770013, L21005770014.

Where was it sold?

Worldwide - US Nationwide distribution in the states of MS, AR, TX, CA, MA, MI, FL, OK, WI, IN, MN, OH, NJ, NY, IL, KY, NV, HI, SD, ID, MI, UT, WA, MO, VA, GA and the countries of DE, CN, JP, UY.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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