CLASS II ONGOING Device recall · Reported 9 Nov 2022 · FDA Enforcement Report
Centurion Medical Products Nicu Picc Insertion Bundle W/o recalled
MEDLINE INDUSTRIES, LP - Northfield is recalling Centurion Medical Products Nicu Picc Insertion Bundle W/o, distributed nationwide in the US. The recall was initiated on 30 Sep 2022 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-0167-2023
- FDA event ID
- 90946
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield, Northfield, IL
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 30 Sep 2022
- FDA classified
- 1 Nov 2022
- Reported
- 9 Nov 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- N/A
- Reason category
- Sterility
- Device type
- Other Medical Devices
Timeline
| 30 Sep 2022 | Recall initiated by company | |
| 1 Nov 2022 | Classified by FDA | +32 days |
| 9 Nov 2022 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal.
A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.
Product as listed by the FDA
CENTURION MEDICAL PRODUCTS NICU PICC INSERTION BUNDLE W/O, REF CVI4470. Convenience kit used in medical procedures.
Where it was distributed
US Nationwide distribution in the states of CA, MN, NC, NY, OK, PA, TN, TX.
Nationwide CaliforniaMinnesotaNorth CarolinaNew YorkOklahomaPennsylvaniaTennesseeTexas
Questions about this recall
Is Centurion Medical Products Nicu Picc Insertion Bundle W/o recalled?
Yes. MEDLINE INDUSTRIES, LP - Northfield recalled Centurion Medical Products Nicu Picc Insertion Bundle W/o on 30 Sep 2022. The recall is Class II and its status is Ongoing. Recall number Z-0167-2023.
Why was it recalled?
Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal.
Which lots are affected?
GTIN (01) 40653160316252, Lot Number 21KBB343
Where was it sold?
US Nationwide distribution in the states of CA, MN, NC, NY, OK, PA, TN, TX.
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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