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Adverse-event reports (MAUDE)

Read this first: MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line shows reporting volume for the average device in the same FDA product code — a reporting baseline, not a risk measure.

1 linked reportInjury 1
11222019-12: 0 reports for this device; peer average 1/device2020-09: 0 reports for this device; peer average 2/device2020-10: 0 reports for this device; peer average 1/device2020-11: 0 reports for this device; peer average 2/device2021-01: 0 reports for this device; peer average 1/device2026-04: 1 reports for this device; peer average 1/device120910110104
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2019-1201
2020-0902
2020-1001
2020-1102
2021-0101
2026-0411
This device (reports/month)Average device in LFD (reports/device/month)
Failure-mode summaryAI-generated

1 linked report narrative available — no AI summary generated yet.

Recall history
InitiatedRecall #ClassStatusReasonQuantityLink basis
2013-10-17Z-0272-2014Class IITerminatedLabel indicates, "Sweetened with xylitol and Sorbitol", however product does not contain sorbitol.Distribution: Nationwide Distribution .483,204 bottlesclearance family
Individual MAUDE reports
DateReport #TypeNarrativeLink basis
2026-04-08MW5186491InjuryAvailableprocode brand trgm
Regulatory clearances
  • 510(k)K123731Substantially equivalent (SESE) · 2013-01-04clearance family

Predicate lineage

K123731

Cited as predicate by: K150074, K152201, K163029, K181134, K181194, K181839, K231205, K240508, K253778

Lineage each submission cites, walked transitively (indented = the cited device's own predicates). Extracted from public 510(k) summary text — heuristic, and includes reference devices mentioned alongside true predicates.

Manufacturer compliance record

None in the loaded window.

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