CLASS II Drug recall · Reported 18 Mar 2020 · FDA Enforcement Report

Ertapenem in 9% NACL 1GM Injectable recalled

Redline Pharmacy Solutions is recalling Ertapenem in 9% NACL 1GM Injectable, Redline Specialty Pharmacy, 2415 Osborne Drive E, distributed in Nebraska. The recall was initiated on 24 Feb 2020 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot 02242020@7
Quantity recalled8 doses

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-1009-2020
FDA event ID
85081
Recalling firm
Redline Pharmacy Solutions, Hastings, NE
Classification
Class II
Status
Terminated
Recall initiated
24 Feb 2020
FDA classified
12 Mar 2020
Reported
18 Mar 2020
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Other Reasons

Timeline

24 Feb 2020Recall initiated by company
12 Mar 2020Classified by FDA+17 days
18 Mar 2020Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Lack Of Processing Controls

Product as listed by the FDA

Ertapenem in 100ML 0.9% NACL 1GM Injectable, Redline Specialty Pharmacy, 2415 Osborne Drive E, #100 Hastings, NE 68901

Where it was distributed

Sold to patients in Nebraska

Nebraska

Questions about this recall

Is Ertapenem in 9% NACL 1GM Injectable, Redline Specialty Pharmacy, 2415 Osborne Drive E recalled?

Yes. Redline Pharmacy Solutions recalled Ertapenem in 9% NACL 1GM Injectable, Redline Specialty Pharmacy, 2415 Osborne Drive E on 24 Feb 2020. The recall is Class II and its status is Terminated. Recall number D-1009-2020.

Why was it recalled?

Lack Of Processing Controls

Which lots are affected?

Lot 02242020@7

Where was it sold?

Sold to patients in Nebraska

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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