Skip to content
Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 81730

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

Open FDA event record

Event summary

Timeline bucket
December 05, 2018
Product types
Drug
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Pharmedium Services, 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

2 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 2

Fentanyl Citrate 2 mcg per mL (100 mcg per 50 mL) and Ropivacaine HCl 0.1% in Sodium Chloride 0.9%, Injection, 50 mL total volume in a 60 mL BD Syringe, Rx Only, PharMEDium Services, LLC. 913 N. Davis Ave. Cleveland, MS 38732 NDC 61553-644-75.

D-0333-2019
Recall number
D-0333-2019
Initiated
December 05, 2018
Classification
Class II
Status
Terminated
Recalling firm
Pharmedium Services, LLC
Quantity
295 50 ml in 60 ml syringes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Sub-potent

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Sub-potent

Code information

Lot: 183220013C Exp. 12/19/2018

Distribution pattern

Nationwide in the USA.

drug · product 2 of 2

Fentanyl Citrate 2 mcg per mL (200 mcg per 100 mL) and Ropivacaine HCl 0.2% in Sodium Chloride 0.9%, Injection, 100 mL total volume in a 150 mL Intravia Bag, Rx Only,PharMEDium Services, LLC. 913 N. Davis Ave. Cleveland, MS 38732. NDC 61553-148-48

D-0334-2019
Recall number
D-0334-2019
Initiated
December 05, 2018
Classification
Class II
Status
Terminated
Recalling firm
Pharmedium Services, LLC
Quantity
295 100 mL in 150 mL Intravia bags

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Sub-potent

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Sub-potent

Code information

Lot: 183230004C Exp. 02/17/2019

Distribution pattern

Nationwide in the USA.