The Recall Desk

FDA (Drugs) recall action 79961

Prescript Pharmaceuticals, Inc. recalled 5 products on 2018-05-23

The FDA (Drugs) publishes a recall like this one as 5 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 5 pages.

Products
5
Announced
2018-05-23
Critical
0
Units
—

Why these products were recalled

Labeling: Not Elsewhere Classified: due to a labeled declaration of; Store at 15¿C to 30¿C (59¿F to 86¿F) which differs from the original manufacturer declaration of; Store at 20¿C to 25¿C (68¿F to 77¿F).

The agency’s own wording, quoted from the enforcement report.

States named across these recalls

1–5 of 5

  • ModerateFDA (Drugs)··2018-05-23

    Prescript Pharmaceuticals Recalls Chlorhexidine Liquid Due to Labeling Error

    Prescript Pharmaceuticals is recalling Chlorhexidine 0.12% liquid due to a storage temperature labeling discrepancy. The product was distributed in California.

    Product
    Chlorhexidine 0.12% liquid, 473 MILLITERS. Rx Only. Mnfct for: XTTRUM Laboratories, Chicago, IL 60609. Mnfct by: pharmaceutical Assoiates, Inc., Greenville, SC 29605. Distrib by: PreScript Pharm. INC., Pleasanton, CA 94588. NDC: 00116-2001-16, Bar Code 1385-38-482
    Category
    Distribution
    1 state
  • ModerateFDA (Drugs)··2018-05-23

    Prescript Pharmaceuticals Recalls Clindamycin Capsules Due to Labeling Error

    Prescript Pharmaceuticals is recalling Clindamycin 300 mg capsules because the storage temperature label differs from the manufacturer's original declaration.

    Product
    Clindamycin 300 mg capsules, USP, 28-count M-Pak containers, Rx Only. Mnfct for: Lannett Co. Inc., Philadelphia, PA 19136. Mnfct. by: Lannett Co. Inc., Philadelphia, PA 19136. Pckgd by PreScript Pharm. Inc., Pleasanton, CA 94566. NDC: 00527-1383-01, Bar Code 0784-28-11
    Category
    Distribution
    1 state
  • ModerateFDA (Drugs)··2018-05-23

    Prescript Pharmaceuticals Recalls Acetaminophen and Codeine Tablets for Labeling Error

    Prescript Pharmaceuticals is recalling specific lots of Acetaminophen and Codeine Phosphate tablets because the storage temperature instructions on the label differ from the original manufacturer's declaration.

    Product
    ACETAMINOPHEN AND CODEINE PHOSPHATE (ACETAMINOPHEN AND CODEINE PHOSPHATE)
    Category
    Distribution
    1 state
  • ModerateFDA (Drugs)··2018-05-23

    Prescript Pharmaceuticals Recalls Acetaminophen with Codeine Tablets for Labeling Error

    Prescript Pharmaceuticals is recalling Acetaminophen 300 mg with Codeine Phosphate 30 mg tablets due to a storage temperature labeling discrepancy.

    Product
    Acetaminophen 300 mg with Codeine Phosphate 30 mg tablets, USP, 20-count M-Pak containers, Rx Only. Mnfct for: Mallinckrodt Inc. Hazelwood, MO 63042. Mnfct by:Mallinckrodt Inc. Hazelwood, MO 63042. Pckgd by PreScript Pharm Inc. Pleasanton, CA 94566 NDC: 00406-0484-10 Bar Code 007
    Category
    Distribution
    1 state
  • ModerateFDA (Drugs)··2018-05-23

    Prescript Pharmaceuticals Recalls Clindamycin Capsules Due to Labeling Error

    Prescript Pharmaceuticals is recalling 50 containers of Clindamycin 150 mg capsules in California due to a storage temperature labeling discrepancy.

    Product
    Clindamycin 150 mg capsules, USP, 30-count M-Pak container. Mnfct by: Lannett Co. Inc., Philadelphia, PA. Mnfct for: Lannett Co. Inc., Philadelphia, PA. Pckgd by PreScript Pharm. Inc. Pleasanton, CA 94566. NC 00527-1382-01, Bar Code 0639-30-176
    Category
    Distribution
    1 state