Codman & Shurtleff, Inc.: 57 recalls on record

Recalls filed with 1 agency: FDA (57).

First recall on record: February 27, 2013. Most recent: October 29, 2014.

Risk classification: Class I: 12 · Class II: 45

Most recent recalls

DateAgencyProduct
October 29, 2014FDACodman Lumbar Drainage Catheter Kit II with EDS 3 (External Drainage System) Catalog Nu…Z-0091-2015
October 29, 2014FDACodman EDS 3 Drainage System (no Ventricular Catheter) (External Drainage System) Catal…Z-0090-2015
October 29, 2014FDACodman EDS 3 Drainage System with Ventricular Catheter (External Drainage System) Catalo…Z-0089-2015
August 20, 2014FDACodman Certas - In Line Valve with SIPHONGUARD¿ Device, Unitized BACTISEAL¿ Catheter and …Z-2191-2014
August 20, 2014FDACodman Certas - In Line Valve only with SIPHONGUARD¿ Device; Product Code: 82-8804 Th…Z-2188-2014
August 20, 2014FDACodman Certas - In Line Valve Only; Product Code: 82-8800 The Codman Certas Programma…Z-2184-2014
August 20, 2014FDACodman Certas - In Line Valve with SIPHONGUARD¿, Unitized Catheter and Accessories; Produ…Z-2190-2014
August 20, 2014FDACodman Certas - In Line Valve with Catheter and Accessories; Product Code: 82-8801 Th…Z-2185-2014
August 20, 2014FDACodman Certas - In Line Valve with SIPHONGUARD¿ Device, Catheter and Accessories; Product…Z-2189-2014
August 20, 2014FDACodman Certas - In Line Valve with Unitized Catheter and Accessories; Product Code: 82-88…Z-2186-2014
August 20, 2014FDACodman Certas - In line Valve with Unitized BACTISEAL¿ Catheter and Accessories; Product …Z-2187-2014
May 21, 2014FDAMedStream Programmable Infusion Pump, 20 mL, Product Code: 91-4200 The MedStream progr…Z-1571-2014
May 21, 2014FDAMedStream Programmable Infusion Pump, 40 mL, Product Code: 91-4201 The MedStream progr…Z-1572-2014
April 23, 2014FDACODMAN CERTAS Programmable Valves, central nervous system shunt, models as follows: 82…Z-1468-2014
February 5, 2014FDACodman Certas Programmable Valve In Line Valve with Catheter and Accessories Product Cod…Z-0859-2014
February 5, 2014FDACodman Certas Programmable Valve In Line Valve with Unitized BactiSeal Catheter and Acces…Z-0860-2014
February 5, 2014FDACodman Certas Programmable Valve In Line Valve only with SiphonGuard Device Product Code…Z-0861-2014
February 5, 2014FDACodman Certas Programmable Valve In Line Valve with SiphonGuard Device, Unitized Bactisea…Z-0864-2014
February 5, 2014FDACodman Certas Programmable Valve In Line Valve with SiphonGuard Device, Catheter and Acce…Z-0862-2014
February 5, 2014FDACodman Certas Programmable Valve In Line Valve with Siphonguard, Unitized Catheter and Ac…Z-0863-2014
February 5, 2014FDACodman Certas Programmable Valve In Line Valve Only Product Code: 82-8800 Product Us…Z-0858-2014
January 29, 2014FDATRUFILL¿ n-Butyl Cyanoacrylate (n-BCA) Liquid Embolic System: One 1 g tube of n-BCA, one…Z-0789-2014
January 29, 2014FDATRUFILL¿ n-Butyl Cyanoacrylate (n-BCA) Liquid Embolic System; Two 1 g tubes of n-BCA, on…Z-0788-2014
October 9, 2013FDAMedStream Refill Kit, U.S (6 units): 91-4288 Product Usage: The Medstream programmabl…Z-2298-2013
October 9, 2013FDAMedStream Programmable Pump; 20ml Pump EMEA 91-4200 Product Usage: The Medstream prog…Z-2300-2013

Questions about this company

How many recalls does Codman & Shurtleff, Inc. have?
Recalert has 57 U.S. recalls on record for Codman & Shurtleff, Inc., published between February 27, 2013 and October 29, 2014.
What was the most recent Codman & Shurtleff, Inc. recall?
FDA recall Z-0091-2015, published October 29, 2014: Codman Lumbar Drainage Catheter Kit II with EDS 3 (External Drainage System) Catalog Number: 82-1738 Indicated for draining cerebrospinal fluid (CFS) and other fluids of similar physical character…
Which agencies have handled Codman & Shurtleff, Inc. recalls?
Codman & Shurtleff, Inc. appears as the recalling firm in recalls from: FDA (57).

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