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Recalls · Brand

Arjo, Inc. dba ArjoHuntleigh recalls

Every recall we track for Arjo, Inc. dba ArjoHuntleigh — 1 in all, all from 2017 — plus the complaints and injury reports the public filed about them.

1recalls

Recalls per year, by danger level

1 recall since 2017.

2017: 1 recall — 1 use caution120172018: 0 recalls20182019: 0 recalls20192020: 0 recalls20202021: 0 recalls20212022: 0 recalls20222023: 0 recalls20232024: 0 recalls20242025: 0 recalls20252026 (to date): 0 recalls2026to date

All FDA recall records for Arjo, Inc. dba ArjoHuntleigh since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.

Recalls per year for Arjo, Inc. dba ArjoHuntleigh, by danger level
YearStop using nowUse cautionLower riskNot yet ratedTotal
201701001
201800000
201900000
202000000
202100000
202200000
202300000
202400000
202500000
2026 (to date)00000

What to do if you have a recalled Arjo, Inc. dba ArjoHuntleigh product

  1. Match the model, catalog or lot number on your device to the recall.
  2. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
  3. Report problems to FDA MedWatch.

See this week’s new recalls.

All Arjo, Inc. dba ArjoHuntleigh recalls

1 shown

Arjo, Inc. dba ArjoHuntleigh recall questions

How many recalls has Arjo, Inc. dba ArjoHuntleigh had?

1 recall from Arjo, Inc. dba ArjoHuntleigh are on record with U.S. safety agencies, from 2017.

What is the most recent Arjo, Inc. dba ArjoHuntleigh recall?

Arjo, Inc. dba ArjoHuntleigh recalls ArjoHuntleigh Flowtron ACS900, medical pump, software V1.099 Device is used to prevent the occurrence of Deep Vein, dated Jun 14, 2017. Every Arjo, Inc. dba ArjoHuntleigh recall is listed on this page, newest first.

What should I do if I have a recalled Arjo, Inc. dba ArjoHuntleigh product?

Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.

How do I get alerts for new Arjo, Inc. dba ArjoHuntleigh recalls?

Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.