CLASS II Device recall · Reported 28 Sep 2022 · FDA Enforcement Report
Diversatek Health, M-Catch Retrieval Nets recalled
Diversatek Healthcare is recalling Diversatek Health, M-Catch Retrieval Nets, distributed nationwide in the US. The recall was initiated on 29 Oct 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-1771-2022
- FDA event ID
- 90776
- Recalling firm
- Diversatek Healthcare, Milwaukee, WI
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 29 Oct 2021
- FDA classified
- 19 Sep 2022
- Reported
- 28 Sep 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Packaging Defects
- Device type
- Surgical Instruments
Timeline
| 29 Oct 2021 | Recall initiated by company | |
| 19 Sep 2022 | Classified by FDA | +325 days |
| 28 Sep 2022 | 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
M-Catch Retrieval Nets, Part Number 1175-01 / Lot Number 001919, that were shipped between 9-27-2021 and 10-22-2021, may contain incorrect inner polybag labeling. The outer package labeling is correct.
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
Diversatek Health, M-Catch Retrieval Nets, Part Number REF 1175-01, Quantity 5 EA/u. Used to endoscopically retrieve severed polyps, tissue samples, food bolus, and foreign bodies in the gastrointestinal tract.
Where it was distributed
US Nationwide distribution.
Questions about this recall
Is Diversatek Health, M-Catch Retrieval Nets recalled?
Yes. Diversatek Healthcare recalled Diversatek Health, M-Catch Retrieval Nets on 29 Oct 2021. The recall is Class II and its status is Terminated. Recall number Z-1771-2022.
Why was it recalled?
M-Catch Retrieval Nets, Part Number 1175-01 / Lot Number 001919, that were shipped between 9-27-2021 and 10-22-2021, may contain incorrect inner polybag labeling. The outer package labeling is correct.
Which lots are affected?
UDI/DI 00816734021361, lot number 001919, 2024-10-31, shipped between 9-27-2021 and 10-22-2021.
Where was it sold?
US Nationwide distribution.
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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