Piccolo Basic Metabolic Panel Plus 400-0031Recalls & reported problems
Abaxis, Inc. · The Piccolo® Basic Metabolic Panel Plus, used with the Piccolo blood chemistry analyzer or Piccolo Xpress® chemistry analyzer, is intended to be used for the in vitro quantitative determination of calcium, chloride, creatinine, glucose, lactate dehydrogenase, magnesium, potassium, sodium, total carbon dioxide, and blood urea nitrogen in a clinical laboratory setting or point-of-care location. This disc is for testing heparinized plasma and serum, only. · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI EABA40000311), received between Mar 6, 2025 and Mar 6, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “High Readings” (1 report).
5 other recalls cover devices cleared under the same FDA submission (K010670, K040115, K051108, K934592, K942782, K950164, K992140, K993211); they may or may not involve this specific model.
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.
Reports received per month
Most reported problems
Device problems
- High Readings1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 6, 2025High Readings; High Readings
A HEALTHCARE PROFESSIONAL REPORTED AN UNEXPECTED HIGH POTASSIUM (K+) RESULT USING THE PICCOLO XPRESS ANALYZER, SERIAL NUMBER (B)(6), AND PICCOLO BASIC METABOLIC PANEL PLUS (BMP+), LOT# 4223AC3. THE PATIENT WAS NOT TREATED. CHEM HIGH/LOW: HIGH. ERROR CODES: CHEM K+ / K+ PROBLEM OR QUESTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21536712 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K010670, K040115, K051108, K934592, K942782, K950164, K992140, K993211. One submission often covers many models, so check the product and lot details in each record.
- Z-2361-2020 · Dec 11, 2019 · TerminatedPiccolo Xpress chemistry analyzer, Model No. 1100-1001, Software version 2.1.55 (NGA)/3.1.35(Jen II)
- Z-1066-2011 · Nov 19, 2010 · TerminatedAbaxis brand Piccolo Comprehensive Metabolic Panel; Used with the Piccolo Blood Chemistry Analyzer or Piccolo xpress Chemistry Analyzer; Catalog/Part Number: 400-0028; Product is
- Z-1155-2010 · Nov 16, 2009 · TerminatedPiccolo Comprehensive Metabolic Panel Reagent Disc, 10-pack box, for use with the Piccolo Blood Chemistry Analyzer or Piccoloxpress Chemistry Analyzer, Catalog No. 400-0028, manufa
- Z-2287-2008 · Apr 21, 2008 · TerminatedPiccolo Chemistry Analyzer software version 6.121 with Electrolyte Panel Lot #8041AC5, model number 400-1022 in polyfoil pouch. Piccolo Electrolyte Panel is a single-use, self-c
- Z-2286-2008 · Apr 21, 2008 · TerminatedPiccolo Chemistry Analyzer software version 6.121 with Comprehensive Metabolic Lot #8111AA5 , Model Number 400-1028 in polyfoil pouch. Piccolo Comprehensive Metabolic Panel is a s
Other Nad Reduction/Nadh Oxidation, Lactate Dehydrogenase devices
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- LDH L-P LD3842Randox Laboratories Limited · Nad Reduction/Nadh Oxidation, Lactate Dehydrogenase1 recall0 reports
- Lactate Dehydrogenase acc. to IFCC ver.2 08057958190Roche Diagnostics GmbH · NAD REDUCTION/NADH OXIDATION, LACTATE DEHYDROGENASE15 reports
- ARCHITECT 2P56-22Abbott GmbH · NAD REDUCTION/NADH OXIDATION, LACTATE DEHYDROGENASE13 reports
- Lactate Dehydrogenase acc to IFCC ver2 3004732122Roche Diagnostics GmbH · NAD REDUCTION/NADH OXIDATION, LACTATE DEHYDROGENASE8 reports
- Alinity 07P7420Abbott GmbH · NAD REDUCTION/NADH OXIDATION, LACTATE DEHYDROGENASE6 reports
- ARCHITECT 2P56-42Abbott GmbH · NAD REDUCTION/NADH OXIDATION, LACTATE DEHYDROGENASE3 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.