Recall Register

Drug recall: Enalapril Maleate Tablets USP, 5 mg, 100 Tablets (10X10) blister cards, 12 cartons in a shipper, Rx, Packaged and…

Class III FDA enforcement event 80389. Recall start date: . Status in the FDA record: Terminated. Termination date: .

Reason for recall, in the words of FDA

Failed Impurities/Degradation Specification; out-of-specification results for the Enalapril DKT degradant

Class III, in the words of FDA

a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences

AMERICAN HEALTH PACKAGING started this drug recall on 25 Jun 2018. The firm address in the FDA record is in Columbus, OH. FDA put the recall in Class III. FDA event 80389 has 1 product record. The first FDA enforcement report date is 18 Jul 2018. The record gives the status Terminated, with the termination date 29 Apr 2020.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Distribution

In the words of FDA.

Lot#166023 products distributed from 12/29/16 to 1/19/17 and Lot#168467 distributed from 4/6/17 to 9/11/17. Distributors are the wholesalers who received the product; others are the Corporate…

Recalling firm

AMERICAN HEALTH PACKAGING, Columbus, OH.

Recalling firm: The firm that the FDA record names for a recall.

Products

1 product record in the event.

FDA event 80389: product records
Recall numberProductQuantityClassStatusReport date
D-0915-2018Enalapril Maleate Tablets USP, 5 mg, 100 Tablets (10X10) blister cards, 12 cartons in a shipper, Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH --- NDC 68084-390-01 Carton [68084-390-11 - Unit Dose]1285 cartons (cartons of 100 individual unit doses)Class IIITerminated18 Jul 2018

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Class III: The lowest of the three FDA recall classes.

The event in context

Drug events that started in 2018
367
Share of these events in Class III
29%
Product records in this event
1Median of the firm: 1
Events of the firm on the register
42

Other events of the firm

Other FDA enforcement events of AMERICAN HEALTH PACKAGING
InitiatedProduct (first record)TypeClassRecords
19 Aug 2026Buprenorphine Sublingual Tablets (C-III), 2 mg, 30 Tablets (3x10), Rx only, Distributed by: American Health Packaging, CDrugClass III1
3 May 2022Nitrofurantoin Capsules, USP (Monohydrate/Macrocrystals), 100 mg, 100 Capsules (10 x 10), 10-count blisters per card, 10DrugClass III1
12 Apr 2022Cyanocobalamin Injection, USP, 1000 mcg per mL, For Intramuscular or Subcutaneous Use Only, 25 x 1 mL Vials, Rx only, MaDrugClass III1
22 Feb 2022Oxycodone Hydrochloride Oral Solution, USP (C-II), 5 mg/5 mL, Delivers 5 mL per Cup, 1 Tray of 10 Cups, Rx Only, For InsDrugClass II1
20 Dec 2021Metoprolol Succinate Extended-Release Tablets, USP 50 mg, 500-count bottle, Rx Only, Manufactured by: Alkem LaboratoriesDrugClass II1
17 Sep 2021GlipiZIDE Extended-Release Tablets, 2.5 mg, 30 Tablets (3 blister cards each with 10 individually blistered doses), Rx oDrugClass II1
15 Sep 2021Valproic Acid Oral Solution, USP, 500 mg/10 mL, 100 10 mL unit dose cups per case, Rx Only, Packaged and Distributed by:DrugClass II1
12 May 2021Sirolimus Tablets 1 mg, 30 Tablets (5 blister cards x 6 unit doses), Rx only, Packaged and Distributed by: American HealDrugClass III1
7 Jan 2021Nitrofurantoin Capsules USP (Monohydrate/Macrocrystals), 100 mg, 100 per carton (10 capsules x 10 blister cards), Rx onlDrugClass II1
10 Jun 2020Nabumetone Tablets, USP, 500 mg, 100 Tablets per carton (10 tablets x 10 blister cards), Rx only, Distributed by: AmericDrugClass III1

AMERICAN HEALTH PACKAGING: all 42 events

Official channels

Cite this page

Recall Register. FDA enforcement event 80389. https://recallregister.com/fda/iii/80389/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA drug enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
Newest FDA report date on the register
23 Sep 2026

FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.

Questions

Where was the product distributed?
The FDA record gives this distribution: Lot#166023 products distributed from 12/29/16 to 1/19/17 and Lot#168467 distributed from 4/6/17 to 9/11/17. Distributors are the wholesalers who received the product; others are the Corporate…
What quantity of product is in FDA event 80389?
The FDA record gives this quantity: 1285 cartons (cartons of 100 individual unit doses)
How many drug recalls of 2018 have the same class?
29% of the 367 drug events that started in 2018 are in Class III.
How many FDA recalls does AMERICAN HEALTH PACKAGING have?
AMERICAN HEALTH PACKAGING is the recalling firm in 42 enforcement events on this register. This event is 1 of them.