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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 80442

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

Open FDA event record

Event summary

Timeline bucket
July 11, 2018
Product types
Drug
Classifications
Class III
Statuses
Terminated
Recalling firm wording
Renaissance Lakewood, 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

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.

drug · product 1 of 3

Fluconazole Injection, USP, Iso-Osmotic Sodium Chloride Diluent, 400 mg in 200 mL (2 mg/mL), 200 mL Single Dose Flexible Container bag, Rx only, Manufactured for: Claris Lifesciences Inc., North Brunswick, NJ 08902; By: Claris Injectables Ltd., Gujarat, India; NDC 36000-003-06.

D-1031-2018
Recall number
D-1031-2018
Initiated
July 11, 2018
Classification
Class III
Status
Terminated
Recalling firm
Renaissance Lakewood, LLC
Quantity
3000 bags

App-derived interpretation

Potency or specification failure reason.potency_specification_failure · v1.0.0
Superpotent

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Superpotent Drug and Failed Stability Specifications: lot out of specification for elevated sodium chloride and elevated water vapor.

Code information

Lot # A061213, Exp 09/18

Distribution pattern

Nationwide and Puerto Rico

drug · product 2 of 3

Fluconazole Injection, USP, Iso-Osmotic Sodium Chloride Diluent, 200 mg in 100 mL (2 mg/mL), 100 mL Single Dose Flexible Container bag, Rx only, Manufactured for: Claris Lifesciences Inc., North Brunswick, NJ 08902; By: Claris Injectables Ltd., Gujarat, India, NDC 36000-002-10.

D-1032-2018
Recall number
D-1032-2018
Initiated
July 11, 2018
Classification
Class III
Status
Terminated
Recalling firm
Renaissance Lakewood, LLC
Quantity
3664 bags

App-derived interpretation

Potency or specification failure reason.potency_specification_failure · v1.0.0
out of specification

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Failed Stability Specifications: lot out of specification for elevated water vapor.

Code information

Lot #: A0A0156, Exp 02/19

Distribution pattern

Nationwide and Puerto Rico

drug · product 3 of 3

Fluconazole Injection, USP, Iso-Osmotic Sodium Chloride Diluent, 200 mg in 100 mL (2 mg/mL), 100 mL Single Dose Flexible Container bag, Rx only, Manufactured for: Claris Lifesciences Inc., North Brunswick, NJ 08902; By: Claris Injectables Ltd., Gujarat, India, NDC a) 36000-002-10 and b) 36000-002-06.

D-1033-2018
Recall number
D-1033-2018
Initiated
July 11, 2018
Classification
Class III
Status
Terminated
Recalling firm
Renaissance Lakewood, LLC
Quantity
12088 bags

App-derived interpretation

Potency or specification failure reason.potency_specification_failure · v1.0.0
Superpotent

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Superpotent Drug: lots out of specification for elevated sodium chloride and fluconazole assay.

Code information

Lot #: a) A060966, A060967, A060965, A061023, Exp 07/18; b) A060962, Exp 02/19

Distribution pattern

Nationwide and Puerto Rico