Data Foundry

Medical device recalls 2024

Baxter PST 500 U — Class II medical device recall Z-2512-2024

Ongoing recall by Baxter Healthcare Corporation, reported 2024-08-14, distributed nationwide. Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction for the PST 500 U Precision Surgi

Recall numberZ-2512-2024
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmBaxter Healthcare Corporation, Deerfield, IL, United States
Recall initiated2024-06-28
Classified2024-08-06
Reported by FDA2024-08-14
DistributedNationwide (US)
Countries outside the USCA
Quantity400 units
UPC / GTIN / UDI-DI00887761973671
Serial numbers107936298, 107936299, 107936300, 107946575, 107946576, 107949857, 107951075, 107952514, 107954982, 108021169, 108023287, 108028575, 108028716, 108028747, 108028798, 108028801, 108028803, 108028817, 108028829, 108028840, 108028846, 108029046, 108029052, 108029053, 108049023 and 375 more
Model numbers4080300

Product

Baxter PST 500 U, Precision Surgical Table, Part number (product code) 4080300

Reason for recall

Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction for the PST 500 U Precision Surgical Table due to a potential issue with loose spring pins in the spindle drives. This can cause the tabletop to unexpectedly tilt or move at any time, even without active use of the surgical table. This could potentially result in unintentional patient movement during surgical procedures and/or preparation for surgical procedures, including transport.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2512-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.