CLASS II Device recall · Reported 27 Nov 2019 · FDA Enforcement Report
Ynhh Scope Kit Kit recalled by Centurion Medical Products
Centurion Medical Products is recalling Ynhh Scope Kit Kit, distributed in Connecticut, Illinois. The recall was initiated on 24 Jun 2019 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-0408-2020
- FDA event ID
- 83359
- Recalling firm
- Centurion Medical Products, Williamston, MI
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 24 Jun 2019
- FDA classified
- 15 Nov 2019
- Reported
- 27 Nov 2019
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Other Medical Devices
Timeline
| 24 Jun 2019 | Recall initiated by company | |
| 15 Nov 2019 | Classified by FDA | +144 days |
| 27 Nov 2019 | 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
Various medical device kits contain MAJOR Nasal Decongestant Spray is being recalled by the manufacturer.
Product as listed by the FDA
YNHH SCOPE KIT Kit Code: MNS10475
Where it was distributed
CT, IL
Questions about this recall
Is Ynhh Scope Kit Kit recalled?
Yes. Centurion Medical Products recalled Ynhh Scope Kit Kit on 24 Jun 2019. The recall is Class II and its status is Terminated. Recall number Z-0408-2020.
Why was it recalled?
Various medical device kits contain MAJOR Nasal Decongestant Spray is being recalled by the manufacturer.
Which lots are affected?
Lot # 2019060750 Exp 08/31/2020 Lot # 2019060450 Exp 08/31/2020 Lot # 2018110550 Exp 05/31/2020
Where was it sold?
CT, 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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