Geritrex Recalls
15 recalls on record · July 22, 2015 to July 31, 2019 · Drugs
Recalls by year
15
19
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
July 31, 2019DrugsFDA
Geritrex, LLC recalls Preferred Plus Dioctyl Liquid Stool Softener (Docusate Sodium), 50mg/5mL, 16 FL. Oz. (1 PT.) 473 mL, Manufactured by RIJ
Hazard: cGMP Deviations: Products may have microbial contamination.
July 31, 2019DrugsFDA
Geritrex, LLC recalls Gericare Geri-Tussin DM, 16 FL OZ (473 mL), Geri-care Phamaceuticals Corp. 1650 63rd Street Brooklyn, NY, NDC 57896-660
Hazard: cGMP Deviations: Products may have microbial contamination.
July 31, 2019DrugsFDA
Geritrex, LLC recalls Ritussin DM Double Strength, 4 FL. OZ. (118 mL), RIJ Pharmaceutical Corporation 40 Commercial Avenue Middletown, NY 1094
Hazard: cGMP Deviations: Products may have microbial contamination.
July 31, 2019DrugsFDA
Geritrex, LLC recalls Preferred Plus Pharmacy Iron Elixir Ferrous Sulfate, 220 mg, 16 fl oz. (473 mL), Distributed by: Geri-care Pharmaceutica
Hazard: cGMP Deviations: Products may have microbial contamination.
July 31, 2019DrugsFDA
Geritrex, LLC recalls Gericare Iron Supplement Elixir Ferrous Sulfate, 220 mg, 16 fl oz. (473 mL), Distributed by: Geri-care Pharmaceuticals C
Hazard: cGMP Deviations: Products may have microbial contamination.
July 31, 2019DrugsFDA
Geritrex, LLC recalls Gericare Diocto Liquid Docusate Sodium Stool Softener, 50 mg/5mL, 16 FL OZ (473 ml), Dist. BY: Gericare Pharmaceuticals
Hazard: cGMP Deviations: Products may have microbial contamination.
July 31, 2019DrugsFDA
Geritrex, LLC recalls Ritussin DM Children & Adults, 4 Fl. Oz. (118 mL), RIJ Pharmaceutical Corporation 40 Commercial Avenue Middletown, NY 10
Hazard: cGMP Deviations: Products may have microbial contamination.
July 31, 2019DrugsFDA
Geritrex, LLC recalls Diphenhydramine Oral Liquid Alcohol Free, 12.5 mg/5 mL, 4 fl oz (118 mL), RIJ Pharmaceutical Corporation 40 Commercial A
Hazard: cGMP Deviations: Products may have microbial contamination.
June 19, 2019DrugsFDA
Geritrex, LLC recalls Senna (sennosides 8.8 mg) Syrup 8 fl oz. (236 mL) bottles, Distributed by Geritrex, LLC 40 Commercial Avenue Middletown,
Hazard: Failed Impurities/Degradation Specifications: Atypical odor and unpleasant taste was reported
June 19, 2019DrugsFDA
Geritrex, LLC recalls Senna (sennosides 8.8 mg) Syrup, 8 fl oz. (237 mL) bottles, Rij Pharmaceuticals Corporation 40 Commercial Avenue, Middle
Hazard: Failed Impurities/Degradation Specifications: Atypical odor and unpleasant taste was reported
December 9, 2015DrugsFDA
Geritrex Corp recalls Polyethylene Glycol 3350-GRX Powder 100% jars a) 8.4 oz (250 g) (NDC 54162-335-02), b) Net wt. 16.9 oz (500 g) (NDC 54
Hazard: Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded.
December 9, 2015DrugsFDA
Geritrex Corp recalls GRx HiCort 25 (hydrocortisone acetate 25 mg) Suppositories, 12-count box, Rx only, Distributed by Geritrex Corporation
Hazard: Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded.
December 9, 2015DrugsFDA
Geritrex Corp recalls Carbo-O-Philic 40 Gel 40% (Urea) NET WT tube, .5 oz (15 g), Rx Only For topical use only, Distributed byGeritrex Corpora
Hazard: Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded.
December 9, 2015DrugsFDA
Geritrex Corp recalls Carbo-O-Philic 40 Cream 40% (Urea) tubes, a) 3 oz (85 g) (NDC 54162-640-03) , b) 7 oz (200 g) (NDC 54162-640-07), Rx Onl
Hazard: Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded.
July 22, 2015DrugsFDA
Geritrex Corp recalls Carb-O-Philic 40 Cream, 40%, a) 3 oz. tube (NDC 54162-640-03) b) 7 oz. tube (NDC 54162-640-07), Rx Only, Manufactured by
Hazard: CGMP Deviation: Poor container closure of the bulk storage container