MaXcess 1564851Recalls & reported problems
Nuvasive, Inc. · MaXcess Retractor, ALL Wide Short · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887517118905), received between Jan 6, 2020 and Jan 6, 2020 — classified as 1 injury.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Unspecified Infection1
- Urinary Retention1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJan 6, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
ON UNKNOWN DATE, A PATIENT UNDERWENT THE FIRST OF A TWO-PART PROCEDURE AN EXTREME LATERAL INTERBODY FUSION AT L1/5 LEVELS VIA A RIGHT SIDED TRANSPSOAS RETROPERITONEAL APPROACH, WHERE THE URETERAL WAS REPORTED AS INJURED. SEVEN DAYS POST PROCEDURE THE SECOND HALF OF THE PROCEDURE, A POSTERIOR FIXATION FROM T12 TO ILIUM WAS COMPLETED WITH NO ADDITIONAL ISSUES REPORTED. DURING FOLLOW-UP, EIGHT DAYS POST-OPERATIVE, DISCHARGE WAS EFFLUXED FROM THE WOUND AND A COMPUTED TOMOGRAPHY REVEALED ABNORMAL ACCUMULATION FLUID AROUND THE RIGHT KIDNEY. 16 DAYS LATER, AN END TO END URETEROURETEROSTOMY WAS SUCCESSFULLY PERFORMED WITH NO POST-OP SYMPTOMS.
Patient problems: Unspecified Infection; Urinary Retention
MAUDE report 9556094 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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