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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 85706

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

Open FDA event record

Event summary

Timeline bucket
May 11, 2020
Product types
Drug
Classifications
Class II
Statuses
Terminated
Recalling firm wording
BIOTA Biosciences LLC

Dossier provenance

Source snapshots represented here

  • openFDA Drug 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.

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

5 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.

drug · product 1 of 5

Sterile Cannabidiol (CBD) 4mg/mL, 10mL vial

D-1326-2020
Recall number
D-1326-2020
Initiated
May 11, 2020
Classification
Class II
Status
Terminated
Recalling firm
BIOTA Biosciences LLC
Quantity
N/A

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA: Product contains unapproved Cannabidiol and Curcumin

Code information

Lot #: 2H071219P, 2H0712019P, 2H07122019P, Exp. Date 7/12/2021

Distribution pattern

Nationwide within the United States and New Zealand

drug · product 2 of 5

Sterile Curcumin, 4mg/mL, 10mL vial

D-1327-2020
Recall number
D-1327-2020
Initiated
May 11, 2020
Classification
Class II
Status
Terminated
Recalling firm
BIOTA Biosciences LLC
Quantity
N/A

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA: Product contains unapproved Cannabidiol and Curcumin

Code information

Lot #: 2H071219CCD, 2H0712019CCD, 2H07122019CCD, Exp. Date 7/12/2021

Distribution pattern

Nationwide within the United States and New Zealand

drug · product 3 of 5

Sterile Cannabidiol (CBD) 50mg/mL, 10mL vial

D-1328-2020
Recall number
D-1328-2020
Initiated
May 11, 2020
Classification
Class II
Status
Terminated
Recalling firm
BIOTA Biosciences LLC
Quantity
N/A

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA: Product contains unapproved Cannabidiol and Curcumin

Code information

Lot #: 101019P, 1010019P,10102019P, Exp. Date 10/10/2021

Distribution pattern

Nationwide within the United States and New Zealand

drug · product 4 of 5

Sterile Cannabidiol (CBD) + Curcumin 50mg/mL, 10 mL vial

D-1329-2020
Recall number
D-1329-2020
Initiated
May 11, 2020
Classification
Class II
Status
Terminated
Recalling firm
BIOTA Biosciences LLC
Quantity
N/A

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA: Product contains unapproved Cannabidiol and Curcumin

Code information

Lot #: 101019PC, 1010019PC, 10102019PC, Exp. Date 10/10/2021

Distribution pattern

Nationwide within the United States and New Zealand

drug · product 5 of 5

Sterile Curcumin 50mg/mL, 10 mL vial

D-1330-2020
Recall number
D-1330-2020
Initiated
May 11, 2020
Classification
Class II
Status
Terminated
Recalling firm
BIOTA Biosciences LLC
Quantity
N/A

App-derived interpretation

Sterility assurance reason.sterility_assurance · v1.0.0
Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA: Product contains unapproved Cannabidiol and Curcumin

Code information

Lot #: 071219CCD, 0712019CCD, 07122019CCD, Exp. Date 7/12/2021

Distribution pattern

Nationwide within the United States and New Zealand