Reported Mar 8, 2017 · Terminated
Duopa (carbidopa and levodopa enteral suspension), 4.63 mg/20 mg per mL, 100 mL cassette, 7 cassettes per carton, Rx…
AbbVie Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: AbbVie Inc. · 1 N Waukegan Rd · North Chicago, IL · 60064-1802
Is this the product you have?
- Duopa (carbidopa and levodopa enteral suspension), 4.63 mg/20 mg per mL, 100 mL cassette, 7 cassettes per carton, Rx Only, AbbVie Inc., North Chicago, IL 60064 --- NDC 0074-3012-07
- Lot codes and dates
- Lots
1055692Expiration Date (Frozen) 06/01/2018 1057881Expiration Date (Frozen) 06/02/2018 1060138Expiration Date (Frozen) 06/13/2018 1060140Expiration Date (Frozen) 06/15/2018 1061258Expiration Date (Frozen) 06/17/2018 1061262Expiration Date (Frozen) 06/30/2018 1063033Expiration Date (Frozen) 07/14/2018
- Lots
- Amount recalled
- 4021 cartons, 7 100-mL cassettes each
Where it was sold
Why it was recalled
Failed Stability Specifications: confirmed out of specification results obtained during refrigerated material stability testing indicating that drug may settle within drug cassettes nearing the end of their refrigerated shelf-life
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new AbbVie Inc. recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.