Recall Atlas
Drugs & medical

Sandoz Recalls Aprepitant Capsules and Lidocaine and Prilocaine Cream Prescription Drugs Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning

The recalled prescription drugs and products that contain lidocaine must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the products is not child resistant,…

Read the official notice → Aprepitant capsules and Lidocaine and Prilocaine cream
Date
2023-03-09
Country
United States
Brand
Sandoz Inc., of Princeton, New Jersey (Lidocaine and…
Product
Aprepitant capsules and Lidocaine and Prilocaine cream
Units
About 156,750
Category
Drugs & medical
Source
CPSC

Copied automatically from the US Consumer Product Safety Commission. Details may be shortened or out of date; the official notice is the authoritative source.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 Consumer Product Safety Commission has the exact models, batch codes and remedy, and it takes priority.

Other drugs & medical recalls in the United States

  1. 2023-03-15
  2. US
    Drugs & medicalClass II

    Sagent Pharmaceuticals Inc recalls Heparin Sodium Injection, USP, 20,000 USP units per mL, 25 x 1 mL Multi-Dose Vials, Rx Only, For Intravenous or Subcutaneous Use, Mfd.…

    Labeling: Not elsewhere classified

    FDA · DrugSagent Pharmaceuticals IncUSA NationwideOfficial notice →
  3. US
    Drugs & medicalClass II

    B. Braun Medical Inc recalls Heparin Sodium, 25,000USP units per 250 mL, (100 USP units per mL) in 5% Dextrose Injection, 250 mL Excel Container, B.Braun Medical Inc,…

    Subpotent Drug: low Anti-Factor IIa potency.

    FDA · DrugB. Braun Medical IncNationwide in the USAOfficial notice →
  4. US
    Drugs & medicalClass II

    Apotex Corp. recalls Brimonidine Tartrate Ophthalmic Solution 0.15%, Rx Only, Packaged as: a) 5 mL dropper bottle, NDC 60505-0564-1, UPC 3 60505 05641 5; b) 10…

    Lack of sterility assurance: Cracks have developed in some of the units caps of Brimonidine tartrate ophthalmic solution bottles. There is a possibility the broken cap may impact sterility.

    FDA · DrugApotex Corp.Nationwide in the USAOfficial notice →
  5. 2023-03-08
  6. US
    Drugs & medicalClass II

    Coltene Whaledent Inc recalls SciCan STATIS SL S10001 Dental Handpieces-Intended for the removal of carious material, reducing hard tooth structure, cavity preparation,…

    Screw connection between the turbine head and the push button may loosen and fall off during the treatment, and increase the risk of swallowing or inhaling part of the turbines head or the push button

    FDA · DeviceColtene Whaledent IncNationwide Foreign: Canada Germany Indonesia Ireland Lebanon Saudia Arabia…Official notice →
  7. US
    Drugs & medicalClass II

    Carestream Health, Inc. recalls DRX-Compass/DR-FIT X-ray Systems with Firmware version 2.3.2.0/2.3.2.4. For use in obtaining diagnostic quality radiographic images to…

    After pressing and releasing the Z-Axis Motorized buttons on the Tube Head Display, the Overhead Tube Crane (OTC) could potentially continue the movement unexpectedly to a certain distance which could potentially…

    FDA · DeviceCarestream Health, Inc.Worldwide distribution - US Nationwide distribution in the states of…Official notice →
  8. US
    Drugs & medicalClass II

    Med-Mizer, Inc. recalls Sit to Stand STS500 Patient Lift

    Risk of boom pivot failing due to the nut securing the boom becoming loose and the bolt to be unsecure to the flange on the side.

    FDA · DeviceMed-Mizer, Inc.Awaiting consignee list from the recalling firm.Official notice →
See all drugs & medical recalls →