Incorrect Expiration Date: The "11/06" expiration date printed on the tray (secondary packaging) is incorrect (it should be 11/2016)
All Recalls
95,114 total recalls in our database
Presence of Particulate Matter
SENSODYNE EXTRA FRESH COMPLETE PROTECTION, 3.4 oz.(96.4 g) tubes, Manufactured by Oratech, South Jordan UTAH 84095, Distributed by GlaxoSmithKline, Consumer Healthcare, L.P., Moon Township, PA 15108, NDC 0135-0572-02
GlaxoSmithkline Consmer Healthcare
Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.
SENSODYNE COMPLETE PROTECTION, 3.4 oz. (96.4 g)tubes, Manufactured by Oratech, South Jordan UTAH 84095, Distributed by GlaxoSmithKline, Consumer Healthcare, L.P., Moon Township, PA 15108, NDC 0135-0573-02
GlaxoSmithkline Consmer Healthcare
Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.
biotene PBF Toothpaste (Plaque-Biofilm Loosening Formula), a) 4.3 oz. (121.9 g) tubes, (NDC 0135-0559-01), bioteneΒΏ PBF Paste, b) 4.5 oz.(127.6 g) tubes, (NDC 0135-0490-02), Manufactured by Oratech, South Jordan, UTAH 84095, Distributed by GlaxoSmithKline, Consumer Healthcare, L.P., Moon Township, PA 15108
GlaxoSmithkline Consmer Healthcare
Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.
biotene Gentle Formula FLUORIDE TOOTHPASTE GENTLE MINT , 4.3 oz.(121.9 g) tubes, Manufactured by Oratech, South Jordan, UTAH, 84095, Distributed by GlaxoSmithKline, Consumer Healthcare, L.P., Moon Township, PA 15108 NDC 0135-0558-01
GlaxoSmithkline Consmer Healthcare
Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.
biotene Gentle Mint Gel, 4.5 oz.(127.6 g) tubes, Manufactured by Oratech, South Jordan, UTAH 84095, Distributed by GlaxoSmithKline, Consumer Healthcare, L.P., Moon Township, PA 15108, NDC 0135-0488-01
GlaxoSmithkline Consmer Healthcare
Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.
Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.
0.9% Sodium Chloride Injection USP, 500 mL in VIAFLEX Plastic Container, Baxter Healthcare Corporation Deerfield, IL 60015, NDC 0338-0049-03.
Baxter Healthcare
Presence of Particulate Matter and Lack of Assurance of Sterility: The firm received a complaint for customer of presence of particulate matter, leaky containers, and missing port protectors.
Presence of Particulate Matter
Rivastigmine Tartrate Capsules, USP 1.5 mg, 60 count bottle, Rx Only, Mfd. By Dr. Reddy's Laboratories Limited, Bachupally, India, NDC 55111-352-60
Dr. Reddy's Laboratories
Failed Dissolution Specifications
SENSODYNE WITH FLUORIDE REPAIR & PROTECT, a) 0.8 oz.(23 g) tubes, (NDC 0135-0548-01); b) 3.4 oz. (96.4 g) tubes, (NDC 0135-0548-02) Manufactured by Oratech, South Jordan, UTAH 84095, Distributed by GlaxoSmithKline, Consumer Healthcare, L.P., Moon Township, PA 15108
GlaxoSmithkline Consmer Healthcare
Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.
Complaints received of the front joint of the spring arm AC 2000 could break at the interface to the monitor.
ReUnion TSA Shoulder System, Standard SR Humeral Head Trial, 48X18, Catalog number 5901-S-4818. Orthopedic manual surgical instrument. Howmedica Osteonics Corp. A Subsidiary of Stryker Corp. Stryker France Non-sterile Made in Cork Ireland
Stryker Howmedica Osteonics
A package labeled as Part #5901-S-4818, Lot MAC7C14, standard humeral head trial, contained part # 5901-E-4818 Lot MAC7C14, offset humeral head trial.
The manufacturer, B. Braun medical France, received endotoxin test results that are out of specification for the peelable sheath (A1537).
GE Optional Laser Centering Device X-ray generator.
GE Inspection Technologies
GE has identified a potential failure to comply with 21 C.F.R. ΒΏ 1040.10 and 21 C.F.R. ΒΏ 1010.2 for the alignment laser centering device.
Complaints received of the front joint of the spring arm AC 2000 could break at the interface to the monitor.
AngioJet products were distributed with an incorrect use-by (expiry) date. The correct date is Nov-2015, but the units are labeled with a use-by date of Dec-2015.
Stryker Orthopaedics received a report that 5537-G-319 No 3. Triathlon TS Plus Tibial Insert X3 Poly 19 mm i insert was in a package labeled as a 5532-G-511 Triathlon PS Stibialism Insert.
A reagent present may produce weak or slow reactions; continued use may result in a failure to identify target species.