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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 80496

3 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
June 29, 2018
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Quasar Bio-Tech, Inc.

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

3 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 3

Baby Quasar Plus, Light Therapy System, packaging, box, sleeve and user manual. Handheld Wrinkles Reduction Device.

Z-2973-2018
Recall number
Z-2973-2018
Initiated
June 29, 2018
Classification
Class II
Status
Terminated
Recalling firm
Quasar Bio-Tech, Inc.
Quantity
6,783 units total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Quasar did not receive FDA clearance for claims of collagen/elastin production as stated on the packaging and in the user manuals.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Quasar did not receive FDA clearance for claims of collagen/elastin production as stated on the packaging and in the user manuals.

Code information

Product Number DPA-023. UPC Code 0 91037 46144 5

Distribution pattern

Nationwide distribution to CA, FL, GA, HI, IL, LA, MD, NE, NY, OH, TX, VA, WA, WI. Worldwide distribution to Australia, China, Netherlands, United Kingdom

device · product 2 of 3

Quasar MD Plus, Light Therapy System, packaging, box, sleeve and user manual. Handheld Wrinkles Reduction Device.

Z-2974-2018
Recall number
Z-2974-2018
Initiated
June 29, 2018
Classification
Class II
Status
Terminated
Recalling firm
Quasar Bio-Tech, Inc.
Quantity
6,783 units total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Quasar did not receive FDA clearance for claims of collagen/elastin production as stated on the packaging and in the user manuals.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Quasar did not receive FDA clearance for claims of collagen/elastin production as stated on the packaging and in the user manuals.

Code information

Product Number DPA-024. UPC Code 0 91037 46143 8

Distribution pattern

Nationwide distribution to CA, FL, GA, HI, IL, LA, MD, NE, NY, OH, TX, VA, WA, WI. Worldwide distribution to Australia, China, Netherlands, United Kingdom

device · product 3 of 3

Pure Rayz, Light Therapy System, packaging, box, sleeve and user manual. Handheld Wrinkles Reduction Device.

Z-2975-2018
Recall number
Z-2975-2018
Initiated
June 29, 2018
Classification
Class II
Status
Terminated
Recalling firm
Quasar Bio-Tech, Inc.
Quantity
6,783 units total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Quasar did not receive FDA clearance for claims of collagen/elastin production as stated on the packaging and in the user manuals.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Quasar did not receive FDA clearance for claims of collagen/elastin production as stated on the packaging and in the user manuals.

Code information

Product Number DPA-026. UPC Code 0 91037 46140 7

Distribution pattern

Nationwide distribution to CA, FL, GA, HI, IL, LA, MD, NE, NY, OH, TX, VA, WA, WI. Worldwide distribution to Australia, China, Netherlands, United Kingdom