Drugs & medicalClass II

Craftmatic Industries, Inc. recalls Craftmatic Model 1 Base for Dual Bed Configurations

A potential for dual-configured beds to separate or slip away from one another.

Read the official notice →
Date
2022-08-10
Country
United States
Brand
Craftmatic Industries, Inc.
Product
Craftmatic Model 1 Base for Dual Bed Configurations
Classification
Class II
Units
US Nationwide distribution - product was not distributed outside of the United…
Category
Drugs & medical
Source
FDA · Device

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 Details may be shortened or out of date; the official notice is the authoritative source.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.

Other drugs & medical recalls in the United States

  1. 2022-08-17
  2. US
    Drugs & medicalClass II

    Glenmark Pharmaceuticals Inc., USA recalls Telmisartan and Hydrochlorothiazide Tablets USP, 80 mg/25 mg, 30 Tablets, Rx Only, Manufactured by: Glenmark Pharmaceuticals…

    Defective Container: Recall of these batches has been initiated due to complaints of difficult to open blister and tablet breaks while opening the blister .

    FDA · DrugGlenmark Pharmaceuticals Inc., USAnationwideOfficial notice →
  3. 2022-08-10
  4. US
    Drugs & medicalClass II

    Neotract Inc recalls UroLift System REF UL400-4, QTY 4 Urolfit System with Handle Release Tool

    There is the potential that during implant deployment, the device may not properly deliver a implant.

    FDA · DeviceNeotract IncUS: AK AL AR AZ CA CO CT DC DE FL GA IA IL IN KS KY LA MA MD ME MI MN MO MS MT…Official notice →
  5. US
    Drugs & medicalClass II

    Turbett Surgical, Inc. recalls Turbett Surgical Container, TS1500

    Devices were subject to unapproved rework processes.

    FDA · DeviceTurbett Surgical, Inc.US Nationwide Nationwide: CO, FL, NC and PA.Official notice →
  6. US
    Drugs & medicalClass II

    Siemens Healthcare Diagnostics, Inc. recalls Atellica CH Iron_2 (Iron_2) is for in vitro diagnostic use in the quantitative determination of iron in human serum and…

    Falsely Elevated Atellica CH Microalbumin_2 (¿ALB_2) Results due to Reagent Carryover from the Iron_2 Assay. This defect occurs only when a microalbumin test is run immediately after an iron test.

    FDA · DeviceSiemens Healthcare Diagnostics, Inc.Worldwide distribution - US Nationwide and the countries of AR, AU, AT, BS,…Official notice →
  7. US
    Drugs & medicalClass II

    St. Jude Medical, Cardiac Rhythm Management Division recalls Merlin 2 PCS MER37000 programmer Model MER3400 software

    The Merlin" 2 PCS model MER3700 is a portable, dedicated programming system designed to interrogate, program, display data from, and test Abbott Medical implantable medical devices during implant and follow-up.

    FDA · DeviceSt. Jude Medical, Cardiac Rhythm Management DivisionUS: AK AL AR AZ CA CO CT DC DE FL GA HI IA ID IL IN KS KY LA MA MD ME MI MN MO…Official notice →
  8. US
    Drugs & medicalClass II

    St. Jude Medical, Cardiac Rhythm Management Division recalls Merlin PCS 3650 programmer Model 3330 software

    There is a potential for programmer software (Merlin PCS) and remote monitoring software application (Merlin.net) to display overestimated predicted battery longevity for certain pacemakers.

    FDA · DeviceSt. Jude Medical, Cardiac Rhythm Management DivisionUS: AK AL AR AZ CA CO CT DC DE FL GA HI IA ID IL IN KS KY LA MA MD ME MI MN MO…Official notice →
See all drugs & medical recalls →