Reported Aug 9, 2023 · Terminated
succinylcholine 200 mg/10 mL (20 mg/mL), Syringe, Rx only, this drug was repackaged by CAPS Inc, 2200 South 43rd Avenue…
Central Admixture Pharmacy Services, 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: Central Admixture Pharmacy Services, Inc. · 2200 S 43rd Ave · Phoenix, AZ · 85043-3909
Is this the product you have?
- succinylcholine 200 mg/10 mL (20 mg/mL), Syringe, Rx only, this drug was repackaged by CAPS Inc, 2200 South 43rd Avenue Pheonix, AZ, NDC 72196-6011-2.
- Lot codes and dates
- Lot
99 of 99 codes
36-23881236-23881336-23881436-23881536-23881636-238819Exp. 7/10/202336-23928136-23928236-239284Exp. 7/11/202336-23945936-23946036-23962836-239629Exp. 7/12/202336-23987936-23988036-239881Exp. 7/13/202336-240272Exp. 7/16/202336-24051236-24051336-24051436-24051536-240724Exp. 7/17/202336-24099136-24099236-240993Exp. 7/18/202336-24126736-241269Exp. 7/19/202336-24136436-24136636-24136736-241368Exp. 7/20/202336-24166936-24167036-241735Exp. 7/21/202336-24207936-24208036-24208136-24208236-24208336-24208436-242085Exp. 7/24/202336-24262436-24262736-24262836-242629Exp. 7/26/202336-24304636-24304736-243048
- Lot
- Amount recalled
- 26,208 Syringes
This recall covers 95 products
The agency filed one notice per product. You are reading one of them; the other 94 are below.
82 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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