Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 0069-0106-01 recalled?

Elelyso · 1 VIAL, GLASS in 1 CARTON (0069-0106-01) / 5 mL in 1 VIAL, GLASS

Yes — this exact package was recalled

2 FDA recalls name the code 0069-0106-01 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.

Active ingredient
Taliglucerase alfa
Strength
TALIGLUCERASE ALFA 200 U/5mL
Form
Injection, Powder, Lyophilized, for Solution · Intravenous
Labeler
Pfizer Laboratories Div Pfizer Inc
Type
Human Prescription Drug
Product code
0069-0106

Recalls naming this package

Class II · Moderate risk

Elelyso (taliglucerase alfa)

Lack of Assurance of Sterility--Reports of loose metal ferrule crimps on vials for injection. The entire cap either lifted or dislodged while attempting to flip off the orange color plastic button.

Terminated Sterility / contamination Pfizer Inc. NDC 0069-0106-01 D-0995-2020
Class II · Moderate risk

Elelyso (taliglucerase alfa)

Lack of assurance of sterility -Reports of loose metal ferrule crimps on vials for injection. The entire cap either lifted or dislodged while attempting to flip off the orange color plastic button.

Terminated Sterility / contamination Pfizer Inc. NDC 0069-0106-01 D-0005-2019

Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.

Other recalled products from this labeler