Sandoz recalls

Sandoz appears in 61 official U.S. recall notices indexed by RecallRadar.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• Ropinirole, extended-release tablets, 2 mg, 90 count bottle, Rx only, Manufactured in India by Sandoz Private Ltd, for Sandoz Inc, Princeto…
  FDA Drug · Class II · 2013-11-13 · Sandoz
  Reason: Cross contamination with other products: Sandoz is recalling certain lots of Ropinirole Extended Release Tablets 2 mg due to the potential presence of carryover coming from the previously manufactured product, mycopheno…
• Hydroxychloroquine Sulfate Tablets, USP, 200 mg, Rx Only, 100 Tablets per bottle, Sandoz Inc., Princeton NJ, 08540, NDC 0781-1407-01
  FDA Drug · Class III · 2013-10-16 · Sandoz
  Reason: Failed Tablet/Capsule Specifications: Sandoz is recalling one lot of Hydroxychloroquine Sulfate Tablets, USP, 200mg, due to illegibility of the logo on some tablets.
• Methotrexate Injection, USP, Preservative-Free, 1 g/40 mL (25 mg/mL), 40 mL Single Dose Vial, Rx only, Manufactured for: Sandoz Inc., Princ…
  FDA Drug · Class I · 2013-08-14 · Sandoz
  Reason: Presence of Particulate Matter: Found during examination of retention samples.
• Introvale (levonorgestrel and ethinyl estradiol) tablets, USP, 0.15 mg/0.03 mg, packaged in 91 day regimen per unit carton, 3 Unit Cartons…
  FDA Drug · Class III · 2013-08-14 · Sandoz
  Reason: Contraceptive tablets out of sequence: Contraceptive tablets out of sequence: Introvale (levonorgestrel and ethinyl estradiol tablets USP 0.15mg/0.03mg) is voluntarily being recalled due to inactive placebo tablets inco…
• Estarylla (Norgestimate and Ethinyl Estradiol) Tablets
  FDA Drug · Class II · 2013-07-24 · Sandoz
  Reason: Contraceptive Tablets out of Sequence: A placebo tablet was found in a row of active tablets.
• Cefazolin, injection, 1 gram per vial, 25 vials per box, sterile, Rx only, single-use vial, Manufactured in Austria by Sandoz GmbH for Sand…
  FDA Drug · Class II · 2013-06-19 · Sandoz
  Reason: Lack of Assurance of Sterility: Sandoz Inc is recalling Cefazolin for Injection, USP 1 gm vials, lot DB2208, due to a customer complaint for broken/cracked vials which was confirmed through review of retained samples.
• Amoxicillin Capsules USP 500 mg, Manufactured in Austria by Sandoz GmbH for Sandoz Inc., Princeton, NJ 08540, Rx only
  FDA Drug · Class II · 2013-05-01 · Sandoz
  Reason: Presence of Foreign Substance, Sandoz is recalling certain lots of Amoxicillin Capsules, USP 500 mg due to potential contamination with fragments of stainless steel wire mesh.
• Syeda (drospirenone and ethinyl estradiol), 3 mg/0.03 mg, 3 x 28 tablet blistercards, combination oral contraceptive tablet, Manufactured b…
  FDA Drug · Class III · 2013-02-13 · Sandoz
  Reason: Tablet/Capsule Imprinted with Wrong ID; a portion of the tablets could contain the incorrect debossing on one side of the tablet U2 instead of U3.
• Children's Cetirizine HCl Chewable Tablets 5 mg, 30 count blister pack, Manufactured in India by Sandoz Private Ltd., for Sandoz Inc., Prin…
  FDA Drug · Class III · 2012-10-24 · Sandoz
  Reason: Impurity/Degradation; exceeded impurity specification at the 8 and 15 month time points (betacyclodextrin ester 1&2)
• Pramipexole Dihydrochloride Tablets, 0.25 mg, 90-count tablets per bottle, Rx only, Manufactured in India by Sandoz Private Ltd., for Sando…
  FDA Drug · Class III · 2012-09-26 · Sandoz
  Reason: Impurities/Degradation Products: An out of specification result for a known impurity of the product occurred during 12 month stability testing.
• Pramipexole Dihydrochloride Tablets, 0.125 mg, 90-count tablets per bottle, Rx only, Manufactured in India by Sandoz Private Ltd., for Sand…
  FDA Drug · Class III · 2012-09-26 · Sandoz
  Reason: Impurities/Degradation Products: An out of specification result for a known impurity of the product occurred during 12 month stability testing.