Reaction profile
The FDA adverse-event record for device failure
68 FDA adverse-event reports reference device failure (VeDDRA 93036). Plate codes and volume neighbourhood below; species, breeds, and drugs follow.
- #1585 of 2,481
- by report volume (all reactions)
- 68
- reports citing this reaction
- 5.9%
- death-coded share
- Unknown
- most-affected species
Release-over-release change
What changed in the latest FDA data snapshot
PlainBreed reconstructed the prior snapshot from dated openFDA partitions through 2025 Q4, then compared it with the 2026-07-27 openFDA export. Device failure has 68 reports now versus 68 in that prior snapshot: 0 the same number of (0.0%).
- Report change
- +0
- Death-coded reports
- +0
- Death-coded share
- −0.0 pts
This compares reported-event counts in two source snapshots. It does not establish a change in real-world risk, product safety, or disease incidence.
Subscribe to Device failure changesFDA AER · VeDDRA plate
Code 93036 VOL-LOW
VOL-LOW · DEATH-PAR · MID-PACK · PHOTO-FINISH · SPECIES-UNKNOWN · DRUG-LEAD · DESK-WIDE · BOOK-FULL
- VOL-LOW 68 reports
- DEATH-PAR 5.9%
- MID-PACK #1585/2481
- PHOTO-FINISH Chewing disorder
- SPECIES-UNKNOWN Unknown · 42
- DRUG-LEAD Device: Suture · 22
- DESK-WIDE 9 breeds
- BOOK-FULL 8/8 fields
Nearest volume peer: Chewing disorder (±0 reports)
Instrument codes from this reaction’s FDA CVM adverse-event extract: volume band, death-coded share, corpus rank, photo-finish peer, lead species, lead drug, breed desk, and book completeness. Not a clinical diagnosis.
Report-volume neighbourhood around Device failure
Highest and lowest poles plus nearest volume peers, not a full 2,500-reaction corpus board reprint.
Device failure: low death-coded share in the FDA AER plate
Signature read: 4 death-coded reports is a thin tail count for Device failure in the CVM extract. Report volume sits in the middle third of the reaction corpus. Death-coded share is lower-third: 4 of 68 reports (5.9% of named reports). Nearest volume peer: Chewing disorder (±0 reports). Lead species Unknown (42). Lead co-reported drug Device: Suture (22).
Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Device: Suture appears in filings alongside this reaction; that is association, not causation. Browse the full reactions index or the about page for how PlainBreed frames FDA CVM extracts.
Species Most Affected
Breeds Most Affected
Associated Drugs
Nationwide reactions with similar profiles
Two openFDA-derived peer sets for Device failure, both floored at ≥50 reports so the neighborhoods stay in the advertised mass (the volume chart above is the unfloored photo-finish strip).
Similar report volume
Nearest other reactions by FDA report count (68 here).
Similar death-coded share
Nearest other reactions by death-coded share (5.9% here), distinct from the volume row.
What to do with this reaction
- Compare Device failure's report profile against similar reactions nationwide. See similar reactions
- Read how death-coded share differs from a mortality rate before drawing conclusions. Understanding adverse events
- Browse the full reaction directory to compare report counts across reaction types. All reactions
A report does not prove a drug caused the reaction; consult a veterinarian before acting on this data.
Source: FDA Center for Veterinary Medicine openFDA Animal & Veterinary Adverse Events (CVM AER) · 2025
Informational only. FDA adverse-event reports are voluntary and do not prove causation; consult a veterinarian before acting on them. Verify with FDA CVM →