FDA Drug recall D-1611-2014

CREON (pancrelipase) Delayed-Release Capsules, Lipase 24,000 USP Units, 250 Capsule Bottles, Rx Only

FDA Drug
Class II
terminated
Published 2014-10-08

On 2014-10-08 the FDA classified a Class II recall of CREON (pancrelipase) Delayed-Release Capsules, Lipase 24,000 USP Units, 250 Capsule Bottles, Rx Only by Abbvie, citing presence of Foreign Tablets/Capsules; Presence of co-mingled LipaCreon 13000.

Read the official FDA Drug notice

Agency	FDA Drug
Recall number	D-1611-2014
Classification	Class II
Status	terminated
Initiated	2014-09-15
Published	2014-10-08
Last updated	2026-09-13 11:51 UTC
Company	Abbvie
Distribution	US

Product

CREON (pancrelipase) Delayed-Release Capsules, Lipase 24,000 USP Units, 250 Capsule Bottles, Rx Only. Marketed by: AbbVie Inc., North Chicago, IL 60064, Product of Germany. NDC 0032-1224-07.

Reason

Presence of Foreign Tablets/Capsules; Presence of co-mingled LipaCreon 13000.

Identifiers

ndc	0032-1203-70
ndc	0032-1203-64
ndc	0032-1206-07
ndc	0032-1206-01
ndc	0032-1206-56
ndc	0032-1212-07
ndc	0032-1212-01
ndc	0032-1212-46
ndc	0032-1212-13
ndc	0032-1224-07
ndc	0032-1224-01
ndc	0032-1224-46
ndc	0032-3016-28
ndc	0032-3016-13
ndc	0032-3016-50
ndc	0032-3016-12
ndc	0032-0045-70
ndc	0032-0045-30
ndc	0032-0046-30
ndc	0032-0046-70
ndc	0032-0047-30
ndc	0032-0047-70
ndc	0032-2636-70
ndc	0032-2636-01
ndc	0032-2636-30
ndc	0032-2637-70
ndc	0032-2637-01
ndc	0032-2637-30
code_info	Lot #: 1020156; Expiry: 3/31/2016

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Other recalls by Abbvie

PRED MILD, prednisolone acetate ophthalmic suspension, USP, 0.12%, 10 mL, Sterile, Rx only, Allergen, Inc., an AbbVie company, North Chicag…
FDA Drug · Class III · 2026-06-03 · Abbvie
Refresh LACRI-LUBE, (42.5% Mineral Oil, 57.3% White Petrolatum) Lubricant Eye Ointment, Net wt, 0.12 oz (3.5g) Tube, Distributed by: Allerg…
FDA Drug · Class II · 2024-10-02 · Abbvie
Refresh P.M., (Mineral Oil 42.5%, White Petrolatum 57.3%) Lubricant Eye Ointment, Net wt, 0.12 oz (3.5g) Tube, Distributed by: Allergen, an…
FDA Drug · Class II · 2024-10-02 · Abbvie
Synthroid, Levothyroxine Sodium Tablets, USP 125mcg (0.125mg), 100-count bottle, Rx Only AbbVie Inc
FDA Drug · Class III · 2023-11-15 · Abbvie
Ultane (sevoflurane), 250 mL, Inhalation Anesthetic, Rx only, Manufactured by: AbbVie Inc., North Chicago, IL 60064, USA. NDC 0074-4456-51
FDA Drug · Class III · 2018-02-07 · Abbvie

All Abbvie recalls

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1611-2014%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.