CLASS II ONGOING Device recall · Reported 8 Oct 2025 · FDA Enforcement Report
Argus PB-3000, Reference Numbers: 1A.701307 recalled by Schiller, Ag
Schiller, Ag is recalling Argus PB-3000, Reference Numbers: 1A.701307 921002, 921030 921031, 921006, distributed nationwide in the US. The recall was initiated on 8 Aug 2025 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-2672-2025
- FDA event ID
- 97451
- Recalling firm
- Schiller, Ag, Baar, N/A
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 8 Aug 2025
- FDA classified
- 29 Sep 2025
- Reported
- 8 Oct 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Other Medical Devices
Timeline
| 8 Aug 2025 | Recall initiated by company | |
| 29 Sep 2025 | Classified by FDA | +52 days |
| 8 Oct 2025 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Vital sign monitoring instrument may trigger an error message during blood pressures measurements, Specifically, when the initial inflation pressure is set in the high-pressure range.
Product as listed by the FDA
Argus PB-3000, Reference Numbers: 1A.701307,3.921002, 3.921030,3.921031, 3.921006
Where it was distributed
US Nationwide distribution in the states of MT, WI, IL.
Questions about this recall
Is Argus PB-3000, Reference Numbers: 1A.701307 921002, 921030 921031, 921006 recalled?
Yes. Schiller, Ag recalled Argus PB-3000, Reference Numbers: 1A.701307 921002, 921030 921031, 921006 on 8 Aug 2025. The recall is Class II and its status is Ongoing. Recall number Z-2672-2025.
Why was it recalled?
Vital sign monitoring instrument may trigger an error message during blood pressures measurements, Specifically, when the initial inflation pressure is set in the high-pressure range.
Which lots are affected?
REF: 1A.701307: UDI- 07613365003024 REF: 3.921002, UDI: 07613365001914 REF: 3.921030, UDI: 07613365003468 REF: 3.921031: UDI: 07613365003475 REF: 3.921006, UDI: 07613365000115 Affected Serial Numbers: 7010.000160 and lower, 7012.000356 and lower, 7013.000256 and lower, 7014.000152 and lower
Where was it sold?
US Nationwide distribution in the states of MT, WI, IL.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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