CLASS II Device recall · Reported 6 Oct 2021 · FDA Enforcement Report
Outlook Pump Primary Administration Set w/ micro Tubing for Epidural recalled
B. Braun Medical is recalling Outlook Pump Primary Administration Set w/ micro Tubing for Epidural, distributed nationwide in the US. The recall was initiated on 10 Aug 2021 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-2559-2021
- FDA event ID
- 88531
- Recalling firm
- B. Braun Medical, Allentown, PA
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 10 Aug 2021
- FDA classified
- 24 Sep 2021
- Reported
- 6 Oct 2021
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Packaging Defects
- Device type
- Infusion Pumps
Timeline
| 10 Aug 2021 | Recall initiated by company | |
| 24 Sep 2021 | Classified by FDA | +45 days |
| 6 Oct 2021 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Leakage of the pump set within the cassette portion of the pump sets, potential for delays in administration of medications, under-delivery or incomplete dosing and bloodstream infections.
Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.
Product as listed by the FDA
Outlook Pump Primary Administration Set w/ micro Tubing for Epidural Administration-single use, for use with the Outlook Safety Infusion System and/or Horizon NXT Pump for infusion of parenteral fluids Ref: V7453
Where it was distributed
Worldwide distribution - US Nationwide distribution and the country of Canada.
Questions about this recall
Is Outlook Pump Primary Administration Set w/ micro Tubing for Epidural recalled?
Yes. B. Braun Medical recalled Outlook Pump Primary Administration Set w/ micro Tubing for Epidural on 10 Aug 2021. The recall is Class II and its status is Terminated. Recall number Z-2559-2021.
Why was it recalled?
Leakage of the pump set within the cassette portion of the pump sets, potential for delays in administration of medications, under-delivery or incomplete dosing and bloodstream infections.
Which lots are affected?
Lot Code: 0061770205 DI: 04046964189388
Where was it sold?
Worldwide distribution - US Nationwide distribution and the country of Canada.
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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