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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 66103

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

Open FDA event record

Event summary

Timeline bucket
August 26, 2013
Product types
Drug
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Leiter's Pharmacy

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

4 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 4

Dextrose 50% Preservative Free SDV Injection Solution, 50 mL Single dose vial, IV Administration, Compounded by Leiter's Compounding Pharmacy, 1700 Park Ave., # 30, San Jose, CA 95126

D-1038-2013
Recall number
D-1038-2013
Initiated
August 26, 2013
Classification
Class II
Status
Terminated
Recalling firm
Leiter's Pharmacy
Quantity
56 vials

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
bacterial contamination
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: Leiter Pharmacy is recalling due bacterial contamination found after investigation at contract testing laboratory discovered that OOS results were reported to customers as passing. Hence the sterility of these products cannot be assured.

Code information

Lot 06072013@49, Exp 9/5/13

Distribution pattern

Nationwide

drug · product 2 of 4

Hyaluron (hyaluronidase) 150 units/mL Preserved Solution, 1 mL, Multi Dose Vial, Compounded by Leiter's Compounding Pharmacy, 1700 Park Ave., # 30, San Jose, CA 95126

D-1039-2013
Recall number
D-1039-2013
Initiated
August 26, 2013
Classification
Class II
Status
Terminated
Recalling firm
Leiter's Pharmacy
Quantity
810 vials

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
bacterial contamination
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: Leiter Pharmacy is recalling due bacterial contamination found after investigation at contract testing laboratory discovered that OOS results were reported to customers as passing. Hence the sterility of these products cannot be assured.

Code information

Lot #: 06122013@9; Exp 9/10/13

Distribution pattern

Nationwide

drug · product 3 of 4

Bevacizumab (Avastin) 2.5mg/0.1mL PF Inj., 0.1 mL syringe, Compounded by Leiter's Compounding Pharmacy, 1700 Park Ave., # 30, San Jose, CA 95126

D-1040-2013
Recall number
D-1040-2013
Initiated
August 26, 2013
Classification
Class II
Status
Terminated
Recalling firm
Leiter's Pharmacy
Quantity
265 vials

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
bacterial contamination
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: Leiter Pharmacy is recalling due bacterial contamination found after investigation at contract testing laboratory discovered that OOS/failed results were reported to customers as passing. Hence the sterility of the products cannot be assured.

Code information

Lot #: 08052013@1, 08052013@4, Exp 11/03/2013

Distribution pattern

Nationwide

drug · product 4 of 4

Lidocaine/Phenylephrine PF 1%/1.5% Injectible vials, 1 mL Single Use Vial, Compounded by Leiter's Compounding Pharmacy, 1700 Park Ave., # 30, San Jose, CA 95126

D-1041-2013
Recall number
D-1041-2013
Initiated
August 26, 2013
Classification
Class II
Status
Terminated
Recalling firm
Leiter's Pharmacy
Quantity
728 vials

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
bacterial contamination
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: Leiter Pharmacy is recalling due bacterial contamination found after investigation at contract testing laboratory discovered that OOS/failed results were reported to customers as passing. Hence the sterility of these products cannot be assured.

Code information

Lot # : 07302013@6 Exp 10/28/13

Distribution pattern

Nationwide