Codman & Shurtleff recalls

Codman & Shurtleff has 59 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 21 Aug 2019. The most frequent reason is sterility.

Total recalls59since 2013

Last 12 months0reported

Class I1220% of total

Ongoing0latest 21 Aug 2019

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 12 20%Class II 47 80%Class III 0 0%

Why codman & shurtleff is recalled

Product types

By year

201912%
201512%
20142339%
20133458%

All codman & shurtleff recalls, newest first

59 total

Reported	Class	Recall	Company	Reason	Where
21 Aug 2019Device	CLASS II	Galaxy G3 Mini Microcoil Delivery System Product No: GLM915030 recalled	Codman & Shurtleff	Other	CA
3 Jun 2015Device	CLASS II	Codman 3000 Series Refill Set- Huber needles recalled	Codman & Shurtleff	Packaging Defects	Nationwide
29 Oct 2014Device	CLASS II	Codman EDS 3 Drainage System with Ventricular Catheter recalled	Codman & Shurtleff	Packaging Defects	Nationwide
29 Oct 2014Device	CLASS II	Codman EDS 3 Drainage System (no Ventricular Catheter) recalled	Codman & Shurtleff	Packaging Defects	Nationwide
29 Oct 2014Device	CLASS II	Codman Lumbar Drainage Catheter Kit II with EDS recalled	Codman & Shurtleff	Packaging Defects	Nationwide
20 Aug 2014Device	CLASS II	Codman Certas - In line Valve recalled by Codman & Shurtleff	Codman & Shurtleff	Packaging Defects	Nationwide
20 Aug 2014Device	CLASS II	Codman Certas - In Line Valve with Unitized Catheter and Accessories recalled	Codman & Shurtleff	Other	Nationwide
20 Aug 2014Device	CLASS II	Codman Certas - In Line Valve with Siphonguard¿ Device recalled	Codman & Shurtleff	Other	Nationwide
20 Aug 2014Device	CLASS II	Codman Certas - In Line Valve with Catheter and Accessories recalled	Codman & Shurtleff	Other	Nationwide
20 Aug 2014Device	CLASS II	Codman Certas - In Line Valve with Siphonguard¿ Device recalled	Codman & Shurtleff	Packaging Defects	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.