CLASS II Device recall · Reported 19 Dec 2012 · FDA Enforcement Report
Quasar Power Pack contains a Baby Quasar and a Baby Blue recalled
Quasar Bio-Tech is recalling Quasar Power Pack contains a Baby Quasar and a Baby Blue, distributed nationwide in the US. The recall was initiated on 25 Oct 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-0519-2013
- FDA event ID
- 63530
- Recalling firm
- Quasar Bio-Tech, Sarasota, FL
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 25 Oct 2012
- FDA classified
- 12 Dec 2012
- Reported
- 19 Dec 2012
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Other Medical Devices
Timeline
| 25 Oct 2012 | Recall initiated by company | |
| 12 Dec 2012 | Classified by FDA | +48 days |
| 19 Dec 2012 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Quasar Bio-Tech is recalling their Baby Quasar, Baby Quasar Pink, Quasar Power Pack, and Quasar MD because the device is unapproved.
Product as listed by the FDA
Quasar Power Pack contains a Baby Quasar and a Baby Blue. The Baby Quasar is an infrared LED lamp. The Baby Blue uses blue LED light to be used in combination with the Baby Quasar to treat acne. The Quasar Power Pack is labeled in part: "***BABY QUASAR & BABY BLUE***QUASAR POWERPACK***FOR YOUTHFUL, RADIANT, CLEAR SKIN***SKIN REJUVENATING SYSTEM WITH SEQUEPULSE PLUS ADVANCED ACNE CLARIFYING SYSTEM***Manufactured by: Quasar Biotech, Inc., BPP101 LAB-003-E, ***Made in the USA with highest quality components and durable aluminum. Five Year Warranty.***"
Where it was distributed
Worldwide distribution: USA (nationwide) including states of: AZ, CA, CO, FL, GA, HI, ID, IL, KS, MD, MI, MN, MO, NC, NJ, NY, NV, OH, OR, TN, TX, UT, VA, and WA; and countries of: Aruba, Canada, Cayman Islands, China, Estonia, Ireland, Malaysia, New Zealand, Singapore, Sweden, Taiwan, and United Kingdom.
Nationwide ArizonaCaliforniaColoradoFloridaGeorgiaHawaiiIdahoIllinoisKansasMarylandMichiganMinnesotaMissouriNorth CarolinaNew JerseyNevadaNew YorkOhioOregonTennessee
Questions about this recall
Is Quasar Power Pack contains a Baby Quasar and a Baby Blue recalled?
Yes. Quasar Bio-Tech recalled Quasar Power Pack contains a Baby Quasar and a Baby Blue on 25 Oct 2012. The recall is Class II and its status is Terminated. Recall number Z-0519-2013.
Why was it recalled?
Quasar Bio-Tech is recalling their Baby Quasar, Baby Quasar Pink, Quasar Power Pack, and Quasar MD because the device is unapproved.
Which lots are affected?
Quasar Power Pack- Model BPP-101 UPC Code 837654050170, Batch # 11253, 11523, 11658, 2382, 13009, 13177, 13186, 13243, 13270, 13306, 13327, 13342, 13459, 13528, 13529, 13635, 13730, 13767.
Where was it sold?
Worldwide distribution: USA (nationwide) including states of: AZ, CA, CO, FL, GA, HI, ID, IL, KS, MD, MI, MN, MO, NC, NJ, NY, NV, OH, OR, TN, TX, UT, VA, and WA; and countries of: Aruba, Canada, Cayman Islands, China, Estonia, Ireland, Malaysia, New Zealand, Singapore, Sweden, Taiwan, and United Kingdom.
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.
More recalls from Quasar Bio-Tech
All 6| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Baby Quasar Plus, Light Therapy System, packaging recalled | Quasar Bio-Tech | Packaging Defects | Nationwide |
| Device | CLASS II | Quasar MD Plus, Light Therapy System, packaging, sleeve recalled | Quasar Bio-Tech | Packaging Defects | Nationwide |
| Device | CLASS II | Pure Rayz, Light Therapy System, packaging, sleeve and user manual recalled | Quasar Bio-Tech | Packaging Defects | Nationwide |
| Device | CLASS II | Quasar MD is an infrared LED lamp that is labeled in part recalled | Quasar Bio-Tech | Temperature Abuse | Nationwide |
| Device | CLASS II | Baby Quasar (Lab-001-D, BQ101) and Baby Quasar Pink recalled | Quasar Bio-Tech | Temperature Abuse | Nationwide |
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