Genentech Inc: 10 recalls on record

Recalls filed with 1 agency: FDA (10).

First recall on record: December 12, 2012. Most recent: June 5, 2024.

Risk classification: Class I: 2 · Class II: 4 · Class III: 4

Most recent recalls

DateAgencyProduct
June 5, 2024FDACathflo activase (ALTEPLASE), 2mg vials, Rx only, Genentech Inc., South San Francisco, CA…D-0509-2024
November 9, 2022FDASusvimo (ranibizumab injection), 100mg/mL, sold together as a) carton containing One Susv…D-0025-2023
May 5, 2021FDAEvrysdi (risdiplam) for oral solution, 60 mg/80mL (0.75mg/mL), 80 mL total volume after c…D-0357-2021
February 21, 2018FDAKlonopin (clonazepam) 0.5 mg Tablets,100-count bottle, Rx only. Made in Canada, Distribut…D-0416-2018
September 27, 2017FDAActivase (alteplase), 100 mg (58 million IU), Lyophilized vial, packaged with 1 single-do…D-1175-2017
April 12, 2017FDACotellic (cobimetinib) Tablets, 20 mg, 63 count bottle, Rx Only, Made in Switzerland. Dis…D-0648-2017
January 30, 2013FDATrastuzumab Kit containing 1 vial Trastuzumab (nominal content: 440 mg); 1 20 mL multiple…D-135-2013
December 26, 2012FDACellCept (mycophenolate mofetil) capsules, 250 mg, packaged in a) 12 x 120-count bottles …D-097-2013
December 12, 2012FDANutropin AQ NuSpin 20 (somatropin (rDNA origin) injection} 20 mg/ 2mL Genentech, South Sa…D-087-2013
December 12, 2012FDANutropin AQ NuSpin 10 (somatropin (rDNA origin) injection} 10 mg/ 2mL Genentech, South Sa…D-088-2013

Questions about this company

How many recalls does Genentech Inc have?
Recalert has 10 U.S. recalls on record for Genentech Inc, published between December 12, 2012 and June 5, 2024.
What was the most recent Genentech Inc recall?
FDA recall D-0509-2024, published June 5, 2024: Cathflo activase (ALTEPLASE), 2mg vials, Rx only, Genentech Inc., South San Francisco, CA 94080, NDC 50242-041-64
Which agencies have handled Genentech Inc recalls?
Genentech Inc appears as the recalling firm in recalls from: FDA (10).

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