fda
15 records
FDA Drug Recall: Preferred Plus Dioctyl Liquid Stool Softener (Docusate Sodium), 50mg/5mL, 16 FL.
2019-07-31
Class II — cGMP Deviations: Products may have microbial contamination.
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FDA Drug Recall: Gericare Geri-Tussin DM, 16 FL OZ (473 mL), Geri-care Phamaceuticals Corp. 1650
2019-07-31
Class II — cGMP Deviations: Products may have microbial contamination.
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FDA Drug Recall: Gericare Diocto Liquid Docusate Sodium Stool Softener, 50 mg/5mL, 16 FL OZ (473
2019-07-31
Class II — cGMP Deviations: Products may have microbial contamination.
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FDA Drug Recall: Diphenhydramine Oral Liquid Alcohol Free, 12.5 mg/5 mL, 4 fl oz (118 mL), RIJ Ph
2019-07-31
Class II — cGMP Deviations: Products may have microbial contamination.
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FDA Drug Recall: Gericare Iron Supplement Elixir Ferrous Sulfate, 220 mg, 16 fl oz. (473 mL), Dis
2019-07-31
Class II — cGMP Deviations: Products may have microbial contamination.
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FDA Drug Recall: Ritussin DM Double Strength, 4 FL. OZ. (118 mL), RIJ Pharmaceutical Corporation
2019-07-31
Class II — cGMP Deviations: Products may have microbial contamination.
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FDA Drug Recall: Ritussin DM Children & Adults, 4 Fl. Oz. (118 mL), RIJ Pharmaceutical Corporatio
2019-07-31
Class II — cGMP Deviations: Products may have microbial contamination.
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FDA Drug Recall: Preferred Plus Pharmacy Iron Elixir Ferrous Sulfate, 220 mg, 16 fl oz. (473 mL),
2019-07-31
Class II — cGMP Deviations: Products may have microbial contamination.
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FDA Drug Recall: Senna (sennosides 8.8 mg) Syrup 8 fl oz. (236 mL) bottles, Distributed by Geritr
2019-06-19
Class II — Failed Impurities/Degradation Specifications: Atypical odor and unpleasant taste was reported
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FDA Drug Recall: Senna (sennosides 8.8 mg) Syrup, 8 fl oz. (237 mL) bottles, Rij Pharmaceuticals
2019-06-19
Class II — Failed Impurities/Degradation Specifications: Atypical odor and unpleasant taste was reported
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FDA Drug Recall: GRx HiCort 25 (hydrocortisone acetate 25 mg) Suppositories, 12-count box, Rx onl
2015-12-09
Class II — Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded.
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FDA Drug Recall: Carbo-O-Philic 40 Cream 40% (Urea) tubes, a) 3 oz (85 g) (NDC 54162-640-03) , b)
2015-12-09
Class II — Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded.
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FDA Drug Recall: Polyethylene Glycol 3350-GRX Powder 100% jars a) 8.4 oz (250 g) (NDC 54162-335-
2015-12-09
Class II — Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded.
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FDA Drug Recall: Carbo-O-Philic 40 Gel 40% (Urea) NET WT tube, .5 oz (15 g), Rx Only For topical
2015-12-09
Class II — Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded.
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FDA Drug Recall: Carb-O-Philic 40 Cream, 40%, a) 3 oz. tube (NDC 54162-640-03) b) 7 oz. tube (NDC
2015-07-22
Class III — CGMP Deviation: Poor container closure of the bulk storage container
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fda_adverse
1 records
ny_corps
1 records
NY Corp: GERITREX CORP.
1987-08-03
DOMESTIC BUSINESS CORPORATION | County: Westchester | Jurisdiction: New York
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