Data Foundry

Medical device recalls 2012

Quasar Power Pack contains a Baby Quasar and a Baby Blue — Class II medical device recall Z-0519-2013

Terminated recall by Quasar Bio-Tech, Inc. dba Silver Bay LLC, reported 2012-12-19, distributed nationwide. Quasar Bio-Tech is recalling their Baby Quasar, Baby Quasar Pink, Quasar Power Pack, and Quasar MD because the

Recall numberZ-0519-2013
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmQuasar Bio-Tech, Inc. dba Silver Bay LLC, Sarasota, FL, United States
Recall initiated2012-10-25
Classified2012-12-12
Reported by FDA2012-12-19
Terminated2013-05-21
DistributedNationwide (US)
Countries outside the USAW, CA, CN, EE, GB, IE, KY, MY, NZ, SE, SG, TW
Quantity7,734 devices
Reason classesunapproved product
UPC / GTIN / UDI-DI00837654050170
Lot numbers11253, 11523, 11658, 13009, 13177, 13186, 13243, 13270, 13306, 13327, 13342, 13459, 13528, 13529, 13635, 13730, 13767, 2382
Model numbersBPP-101

Product

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.***"

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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0519-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.