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  1. FDA Recalls
  2. ›Drug Recalls

FDA Drug Recalls

Recalls of prescription drugs, over-the-counter medications, and compounded pharmaceuticals.

Classification
AllClass IClass IIClass III
Status
AllOngoingCompletedTerminated
Date
All timePast 30 daysPast 12 months

Showing 6641–6660 of 17,773 recalls

Class IITerminated

PF-Fentanyl Citrate 2 mcg/mL* & Ropivacaine HCl 0.1% in 0.9% Sodium Chloride Injection-200 mL Total Dose: (400 mcg/200 mg)/200 mL, Rx Only Nephron 503B Outsourcing Facility 4500 12th St. Extension West Columbia, SC 29172 NDC: 69374-526-20

Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

GMP Deviations: potential glass contamination

October 9, 2019 · DrugView details →
Class IITerminated

Rifampin for Injection, USP, 600 mg/vial, Rx only, Manufactured for: Mylan Institutional LLC, Rockford, IL 61103; NDC 67457-445-60.

Mylan Laboratories Limited (Sterile Products Division)

Failed Impurities/Degradation Specifications: discoloration due to elevated unknown impurity results which could decrease the effectiveness of the product.

October 7, 2019 · DrugView details →
Class IIITerminated

Methylphenidate Hydrochloride Oral Solution 5mg per 5mL, 500 mL Bottle, Sugar Free Alcohol Free, Rx Only, Mfd by: KVK Tech, Inc., Newtown, PA 18940, NDC 10702-0163-50.

KVK-Tech, Inc.

Presence of Foreign Substance; Fiber particles.

October 4, 2019 · DrugView details →
Class IITerminated

10% LMD in 5% Dextrose Injection Dextran 40 in Dextrose Injection, USP, 500 mL bags, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7418-13

Pfizer Inc.

Lack of Assurance of Sterility: Bag has the potential to leak.

October 2, 2019 · DrugView details →
Class IIITerminated

Motion Sickness (meclizine hydrochloride) 25 mg tablets, 12-count box, Distributed by Sato Pharmaceutical INC. 20695 S. Western Ave., Suite 240 Torrence, CA 90501, NDC 59779-534-01. UPC 050428345535

Sato Pharmaceutical Inc.

Subpotent Drug

October 1, 2019 · DrugView details →
Class IICompleted

Ranitidine Tablets, USP 150 mg, a.) 65 count bottles (NDC 49035-404-61) b.) 130 count bottles (NDC 49035-404-13) c.) 220 count bottles (NDC 49035-404-65) (Walmart) OTC

Dr. Reddy's Laboratories, Inc.

CGMP Deviations: Presence of NDMA impurity detected in product.

October 1, 2019 · DrugView details →
Class IIITerminated

Sankaijo BOTANICAL LAXATIVE (docusate sodium 8.33 mg and sennosides 1.36 mg) tablets, 150-count bottles, Manufactured by SATO PHARMACEUTICAL CO., LTD., 1-5-27 Motoakasaka Minato-KU Tokyo, Japan; SATO PHARMACEUTICAL, INC., 20695 S. Western Ave., Suite 240, Torrance, CA 90501; NDC 49873-404-01.

Sato Pharmaceutical Inc.

Subpotent Drug: Formulated amount of sennosides component is less than labelled claim.

October 1, 2019 · DrugView details →
Class IICompleted

Ranitidine Tablets 75 mg, a.) 30 count bottles (NDC 63868-482-30), 60 count bottles (NDC 63868-482-60) (CDMA) OTC

Dr. Reddy's Laboratories, Inc.

CGMP Deviations: Presence of NDMA impurity detected in product.

October 1, 2019 · DrugView details →
Class IICompleted

Ranitidine Tablets, USP 150 mg, 40 count bottles, NDC 11673-849-40 (Target) OTC.

Dr. Reddy's Laboratories, Inc.

CGMP Deviations: Presence of NDMA impurity detected in product.

October 1, 2019 · DrugView details →
Class IIITerminated

Motion Sickness Strips (meclizine hydrochloride) 25 mg strips, 8-count box, Distributed by Sato Pharmaceutical INC. 20695 S. Western Ave., Suite 240 Torrence, CA 90501, NDC 69842-288-01. UPC 5042849946

Sato Pharmaceutical Inc.

Subpotent Drug

October 1, 2019 · DrugView details →
Class IICompleted

Ranitidine Tablets, USP 75 mg 30 count bottles (NDC 30142-131-30) (Kroger)

Dr. Reddy's Laboratories, Inc.

CGMP Deviations: Presence of NDMA impurity detected in product.

October 1, 2019 · DrugView details →
Class IICompleted

Ranitidine Tablets, USP 75 mg, NDC 57896-715 (GeriCare) OTC.

Dr. Reddy's Laboratories, Inc.

CGMP Deviations: Presence of NDMA impurity detected in product.

October 1, 2019 · DrugView details →
Class IICompleted

Ranitidine Tablets, USP 150 mg, a.) 24 count bottles (NDC 63868-480-24), b.) 50-count bottles (NDC 63868-480-50) (CDMA) OTC

Dr. Reddy's Laboratories, Inc.

CGMP Deviations: Presence of NDMA impurity detected in product.

October 1, 2019 · DrugView details →
Class IIITerminated

WAL-DRAM 2 (meclizine Hydrochloride) 25 mg tablets, packaged in a) 12 count (NDC 0363-1407-01, UPC 3 11917-18328 2 ) and b) 18-count boxes (NDC 0363-1407-02, UPC 3 11917-20318 8) Distributed by Sato Pharmaceutical INC. 20695 S. Western Ave., Suite 240 Torrence, CA 90501,

Sato Pharmaceutical Inc.

Subpotent Drug

October 1, 2019 · DrugView details →
Class IICompleted

Ranitidine Tablets, USP 75 mg, a.) 30- count bottles (NDC 0363-0131-30), b.) 80-count bottles (NDC 0363-0131-80) (Walgreens) OTC

Dr. Reddy's Laboratories, Inc.

CGMP Deviations: Presence of NDMA impurity detected in product.

October 1, 2019 · DrugView details →
Class IICompleted

Ranitidine Tablets, USP 150 mg, NDC 57896-717 (GeriCare) OTC

Dr. Reddy's Laboratories, Inc.

CGMP Deviations: Presence of NDMA impurity detected in product.

October 1, 2019 · DrugView details →
Class IICompleted

Ranitidine Tablets, USP 150 mg, a.) 24 count bottles (NDC 30142-505-34), b.) 50 count bottles (NDC 30142-505-50) (Kroger) OTC

Dr. Reddy's Laboratories, Inc.

CGMP Deviations: Presence of NDMA impurity detected in product.

October 1, 2019 · DrugView details →
Class IICompleted

Ranitidine Tablets, USP 150 mg, 190 count bottles (2x95) Tray (Sam's Club) OTC, NDC 150062076 UPC Code 078742089720

Dr. Reddy's Laboratories, Inc.

CGMP Deviations: Presence of NDMA impurity detected in product.

October 1, 2019 · DrugView details →
Class IIITerminated

Zentrip (meclizine Hydrochloride), 25 mg strips, 8-strips per box, Distributed by Sato Pharmaceutical INC. 20695 S. Western Ave., Suite 240 Torrence, CA 90501, NDC 49873-803-01. UPC 4987301603

Sato Pharmaceutical Inc.

Subpotent Drug

October 1, 2019 · DrugView details →
Class IICompleted

Ranitidine Tablets, USP 150 mg, a.) 95 count bottles (NDC 43598-808-62), b.) 220 count bottles (NDC 43598-808-65) (HCA) OTC.

Dr. Reddy's Laboratories, Inc.

CGMP Deviations: Presence of NDMA impurity detected in product.

October 1, 2019 · DrugView details →
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