Drugs & medicalClass I

Draeger Medical, Inc. recalls Brand Name: Atlan Product Name: Atlan A300XL Model/Catalog Number: 8621400 The Atlan is an anesthesia workstation intended for use in…

The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.

Read the official notice →
Date
2024-12-25
Country
United States
Brand
Draeger Medical
Product
Brand Name: Atlan Product Name: Atlan A300XL Model/Catalog Number: 8621400 The Atlan is an anesthesia workstation intended for use in…
Classification
Class I
Units
No Atlan A300 or A300XL devices were imported into the US. Devices were direct…
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 Details may be shortened or out of date; the official notice is the authoritative source.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.

More Draeger Medical recalls

  1. 2024-11-20
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    Draeger Medical, Inc. recalls Brand Name: Atlan Product Name: Atlan A350XL Model/Catalog Number: 8621600 Software Version: Not Applicable Component: Not applicable

    The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.

    FDA · DeviceDraeger Medical, Inc.US Nationwide distribution in the states of AL, AZ, CA, FL, GA, IA, IL, KY,…Official notice →
  3. 2024-04-24
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    Draeger Medical, Inc. recalls Dr¿ger Perseus A500 Anesthesia Workstation

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    FDA · DeviceDraeger Medical, Inc.Domestic: Nationwide Distribution; Foreign: Angola, Argentina, Australia,…Official notice →
  5. 2023-08-30
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    Draeger Medical, Inc. recalls Carina Sub-Acute Care Ventilator

    Presence of polyether polyurethane (PE-PUR) and emission of 1,3-Dichloropropan-2-ol that exceed the acceptable uptake level during continuous use (>30 days) in pediatric patients.

    FDA · DeviceDraeger Medical, Inc.US Nationwide Distribution.Official notice →
  7. 2023-07-19
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    Draeger Medical, Inc. recalls Oxylog 3000 Plus emergency and transport ventilator

    Draeger has become aware of instances where the device stopped working when in use when transitioning from battery to AC operation.

    FDA · DeviceDraeger Medical, Inc.Distributed Nationwide. OUS Distribution: Afghanistan, Algeria, Andorra,…Official notice →
  9. 2023-05-24
  10. US
    Drugs & medicalClass I

    Draeger Medical, Inc. recalls VentStar Basic (P)180, MP00351

    Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.

    FDA · DeviceDraeger Medical, Inc.Domestic: US Nationwide Distribution.Official notice →
  11. 2023-03-01
  12. US
    Drugs & medicalClass I

    Draeger Medical, Inc. recalls NovaStar TS, Standard elbow, Reusable, Material Numbers MP01579 (Size S), MP01580 (Size M), and MP01581 (Size L)

    The magnets used in the swivel frame/tube set and the headgear clips might impact medical devices (implanted as well as not implanted) and metallic implants.

    FDA · DeviceDraeger Medical, Inc.US Nationwide DistributionOfficial notice →
All 11 Draeger Medical recalls →

Other drugs & medical recalls in the United States

  1. 2024-12-25
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    Philips North America Llc recalls Philips Smart-Hopping 2.0 AP 1.4 GHz. Model Number: 867216

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    FDA · DevicePhilips North America LlcNationwide distributionOfficial notice →
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    Spacelabs Healthcare, Ltd. recalls Eclipse PRO REF 98700 The Spacelabs model 98700 is a portable non-invasive Holter recorder intended to record the patient s ambulatory…

    Due to a manufacturing error the incorrect device serial number was potentially programmed into the holter recorder. The physical serial number label on the device might not match the serial number programmed into the…

    FDA · DeviceSpacelabs Healthcare, Ltd.U.S.: AR, CA, CO, DE, FL, FA, LA, MA, MI, MN, MT, NC, NE, NU OH, OR, PA,…Official notice →
  4. US
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    Spectranetics Corporation recalls Turbo Elite Laser Atherectomy Catheter Model Number / UDI-DI code / Product Description 414-151 / 989930000531 / 1.4 mm OTW 417-152 /…

    Due to complaints received for the marker band detaching from the distal tip of the catheter and remaining in the patient as laser catheter was retracted.

    FDA · DeviceSpectranetics CorporationU.S.: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, ILIN, KS, KY,…Official notice →
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    Medtronic Neurosurgery recalls Exacta External Drainage and Monitoring System: 27581 KIT 27581 EXACTA W/EDM VCATH 35CM 27636 EDM 27636 EXACTA W/BRAIDED CORD LOCK 27666…

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  6. US
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    Kirwan Surgical Products, LLC recalls Optikon Bipolar Pencil 25 Gauge Straight. Model/Catalog Number: OPT14-5011. Product Description: The Disposable Microsurgical…

    Potential for the outer stainless-steel tube to break or detach.

    FDA · DeviceKirwan Surgical Products, LLCWorldwide - US Nationwide including PUERTO RICO; AUSTRALIA, CANADA, CHILE,…Official notice →
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    Macleods Pharmaceuticals Ltd recalls Olanzapine Tablets, USP 2.5 mg, 30-count bottle, Rx Only, Manufactured for: Macleods Pharma USA, Inc. Princeton, NJ 08540,…

    Failed Impurities/Degradation Specifications

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See all drugs & medical recalls →