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ESR RACK N/BACK PANEL

Sarstedt Aktiengesellschaft & Co.KG · Model 90.1060.062 · UDI-DI 04038917124935

JPH
7
510(k) clearances
14
Adverse events
1
Recalls
13
Facilities

Recalls

DateFirmReason
2026-08-25POLYMEDCO, INC. / POLYMEDCO CANCER DIAGNOSTIC PRODUCTS, LLCDuring use of an affected tube, the operator may encounter increased resistance when inserting the pipette. The resulting pressure buildup may cause the tube cap to detach or be fo

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.