CLASS II Device recall · Reported 22 Aug 2012 · FDA Enforcement Report
BeautyAngel Health Fitness Natural Collagen Stimulation recalled
JK Products & Services is recalling BeautyAngel Health Fitness Natural Collagen Stimulation Anti Aging For human use, distributed nationwide in the US. The recall was initiated on 7 May 2012 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-2183-2012
- FDA event ID
- 61855
- Recalling firm
- JK Products & Services, Jonesboro, AR
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 7 May 2012
- FDA classified
- 10 Aug 2012
- Reported
- 22 Aug 2012
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Other Medical Devices
Timeline
| 7 May 2012 | Recall initiated by company | |
| 10 Aug 2012 | Classified by FDA | +95 days |
| 22 Aug 2012 | 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
The Beauty Angel was marketed without a 510k.
Product as listed by the FDA
BeautyAngel Health Fitness Natural Collagen Stimulation Anti Aging For human use.
Where it was distributed
Worldwide Distribution - USA (nationwide) and Canada
Questions about this recall
Is BeautyAngel Health Fitness Natural Collagen Stimulation Anti Aging For human use recalled?
Yes. JK Products & Services recalled BeautyAngel Health Fitness Natural Collagen Stimulation Anti Aging For human use on 7 May 2012. The recall is Class II and its status is Terminated. Recall number Z-2183-2012.
Why was it recalled?
The Beauty Angel was marketed without a 510k.
Which lots are affected?
All Beauty Angel Models and Serial Numbers Part Numbers 80000904301 and 8001110201.
Where was it sold?
Worldwide Distribution - USA (nationwide) and 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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