Recall Atlas
Drugs & medicalClass II

Safecor Health, LLC recalls Metoclopramide Tablets, USP, 5 mg, 100 Tablets per bottle, Rx Only, Manufactured for: Teva Pharmaceuticals, Parsippany, NJ 07054. NDC:…

Manufacturer is recalling batches due to co-mingled tablet.

Read the official notice →
Date
2026-11-04
Country
United States
Brand
Safecor Health
Product
Metoclopramide Tablets, USP, 5 mg, 100 Tablets per bottle, Rx Only, Manufactured for: Teva Pharmaceuticals, Parsippany, NJ 07054. NDC:…
Classification
Class II
Units
US Nationwide
Category
Drugs & medical
Source
FDA · Drug

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More Safecor Health recalls

  1. 2026-09-23
  2. 2026-05-27
  3. Drugs & medicalClass II

    Safecor Health, LLC recalls Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement Oral Liquid, Contains: Folic Acid 799 mcg/5mL, Delivers 5 mL per oral…

    Presence of a Foreign Substance; black particles observed in liquid

    FDA · DrugSafecor Health, LLCOHOfficial notice →
  4. Drugs & medicalClass II

    Safecor Health, LLC recalls Atomoxetine Capsules HCL, 10 mg Capsules in unit dose foil strip, strips are packed in cartons of 100, Rx Only, Pkg by: Safecor, Columbus,…

    Labeling: Label Mix-Up: Atomoxetine HCl 25mg Capsule incorrectly labeled as Atomoxetine HCl 10mg Capsule.

    FDA · DrugSafecor Health, LLCTX onlyOfficial notice →
  5. 2025-12-10
  6. Drugs & medicalClass II

    Safecor Health, LLC recalls Haloperidol Lactate Injection, 5 mg/mL, 25 x 1 mL Single-Dose Vials, Sterile, Rx only, For Intramuscular Use Only, Manufactured for: Mylan…

    Labeling: Not Elsewhere Classified:Incorrect RFID tag labels applied to product by repackaging firm.

    FDA · DrugSafecor Health, LLCDistributed in MassachusettsOfficial notice →
  7. 2025-03-12
  8. Drugs & medicalClass II

    Safecor Health, LLC recalls Ergocalciferol - Vitamin D Supplement - 10 mcg (400 Units) per 0.05 mL Oral Syringe, Delivers: 0.05 mL Oral Solution, Mfg by: Westminster,…

    Defective Delivery System: Leakage observed after oral solution was repackaged into unit-dose syringes.

    FDA · DrugSafecor Health, LLCNationwide in the USAOfficial notice →
  9. 2024-11-27
  10. Drugs & medicalClass II

    Safecor Health, LLC recalls Aspirin Chewable tablet 81 mg, 1 tablet in blister card-foils, 100-count unit dose box, www.safecorhealth.com, NDC 48433-129-01

    cGMP Deviations: Observations were made that some blister card-foils were separating from the blister cavity.

    FDA · DrugSafecor Health, LLCUSA nationwide.Official notice →
All 8 Safecor Health recalls →

Other drugs & medical recalls in the United States

  1. 2026-11-04
  2. Drugs & medicalClass III

    Prodose, Inc. recalls ValuHealth Extra Strength Pain Relief Acetaminophen 500 mg, 40-caplets per bottle, Distributed by:Prodose, Inc. Ronkonkoma, NY 11779, Made…

    Incorrect label placed on product: Outer carton label correctly identifies drug product in bottle as ValuHealth Extra Strength Pain Relief Acetaminophen 500 mg,but inner label on bottle says ValuHealth Extra Strength…

    FDA · DrugProdose, Inc.Nationwide in the USAOfficial notice →
  3. Drugs & medicalClass II

    Huons Co., Ltd. recalls Carboxymethylcellulose Sodium, 0.5% Lubricant Eye Drops, Sterile, 30 Single-Use Containers, 0.02 FL OZ (0.5 mL) each, Manufactured by:…

    Failed Impurities/Degradation Specification; detection of polyethylene (PE)-related oligomers

    FDA · DrugHuons Co., Ltd.Nationwide within U.S.Official notice →
  4. Drugs & medicalClass II

    Glenmark Pharmaceuticals Inc., USA recalls Abiraterone Acetate Tablets USP 500 mg, 60-count bottles, Rx only, Distributed by: Glenmark Pharmaceuticals USA, Elmwood…

    Labeling: Not Elsewhere Classified

    FDA · DrugGlenmark Pharmaceuticals Inc., USANationwide within the United StatesOfficial notice →
  5. Drugs & medicalClass II

    The Ritedose Corporation recalls Formoterol Fumarate Inhalation Solution, 20mcg/2mL, packaged in cartons of 30 individually wrapped vials (NDC 76204-030-01) and 60…

    Failed Impurities/Degradation Specification

    FDA · DrugThe Ritedose CorporationNationwide within the U.SOfficial notice →
  6. Drugs & medicalNot Yet Classified

    Trifluent Pharma LLC recalls Tridacaine III / Lidocaine Patch 5%, 15 envelopes containing 1 patch each per pouch, Rx only, Distributed by: Trifluent Pharma San…

    Labeling: Incorrect or Missing Lot and/or Exp Date. Incorrect expiration date printed on the label.

    FDA · DrugTrifluent Pharma LLCUSOfficial notice →
See all drugs & medical recalls →