Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy

Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

ยฉ 2026 Go Backs. All rights reserved.

Medium RiskFDA Vet
Medical Devices/Home Healthcare

Aerogen Ltd.: Aeroneb Nebulizer Power Adapters Recalled for Shock Risk

Agency Publication Date: June 30, 2015
Share:
Sign in to monitor this recall

Summary

Aerogen Ltd. is recalling 4,003 FRIWO power adapters used with Aeroneb Solo and Pro Nebulizer systems due to a defect where the adapter cover can break or detach from the main body. This recall involves multiple model and lot numbers distributed across the United States and internationally. While the device is intended to aerosolize physician-prescribed solutions for inhalation in adult and pediatric patients, a small number of complaints have identified that the power adapter cover had broken or dislodged before use. Consumers should immediately check if their specific model and lot number are included in this recall.

Risk

A broken or dislodged power adapter cover can expose internal electrical components, posing a risk of electric shock or device failure during medical treatment. A small number of complaints regarding broken covers have been reported.

What You Should Do

  1. Identify your device by checking the FRIWO AC/DC Adapter for Model Number GPP10, which was supplied with Aeroneb Nebulizer Pro and Solo systems.
  2. Check your specific unit against the extensive list of affected model and lot numbers, such as Model AG-AP1040-US (Lots 8002140520090 through 8002140722093) and Model AG-AS3000-US (Lots 9121140521090 through 9121140709030).
  3. Inspect the power adapter cover for any signs of cracking, loosening, or detachment from the body of the adapter.
  4. If your lot number matches the recall list or if the adapter shows signs of damage, stop using the power adapter immediately and contact your healthcare provider or Aerogen Ltd. for guidance on obtaining a safe replacement.
  5. Contact your healthcare provider or the manufacturer, Aerogen Ltd., for further instructions on receiving a replacement and how to safely return the affected power supply.
  6. For additional questions or to report further issues, contact the FDA Consumer Complaint Coordinator or the agency hotline at 1-888-463-6332.

Your Remedy Options

๐Ÿ“‹Other Action

Contact healthcare provider or manufacturer.

How to: Contact your healthcare provider or the manufacturer for further instructions and potential refund

Affected Products

Product: Aeroneb Professional Nebulizer System - Pro Family (FRIWO GPP10 Adapter)
Model:
AG-AP1040-AU
AG-AP1040-EU
AG-AP1040-UK
AG-AP1040-US
AG-AP1500-IN
AG-AP1500-UK
AG-AP1500-US
AG-AP6000(DG)-FR
AGAP6000(DG)-GE
AG-AP6000(DG)-IN
AG-AP6000-AU
AG-AP6000-CH
AG-AP6000-FR
AG-AP6000-GE
AG-AP6000-IN
AGAP6000-IT
AG-AP6000-NO
AG-AP6000-RU
AG-AP6000-SP
AG-AP6000-SW
AG-AP6000-UK
AG-AP6000-US
Lot Numbers:
8003140519057
8003140708015
8003140722089
800140731124
8000140520074
8000140520087
8002140520090
8002140521088
8002140722093
9939140522091
9913140520026
9902140616065
9902140617070
Product: Aeroneb Solo Nebulizer System (FRIWO GPP10 Adapter)
Model:
AG-AS3000-AU
AG-AS3000-IN
AG-AS3000-NE
AG-AS3000-SC
AG-AS3000-SE
AG-AS3000-UK
AG-AS3000-US
AGPX1000-IN
AG-PX1000-NE
AG-PX1000-SC
AG-PX1000-SE
AG-PX1000-UK
AGPX1000-US
AG-PX1000-US-Promo
Lot Numbers:
9144140519057
9125140522116
9122140520089
9121140521090
9121140709030
9129140527093
9129140617071
Product: Aeroneb Nebulizer System - Additional Models (FRIWO GPP10 Adapter)
Model:
1079422
1082693
1082694
Lot Numbers:
9070140620088
9070140723088
9073140618134
9074140530079
Product: Aeroneb Ultra/Control Systems (FRIWO GPP10 Adapter)
Model:
AG-UC1000-NE
AG-UC1000-UK
AG-UC1500-NE
AG-UC1500-SC
AG-UC1500-SE
Lot Numbers:
9263140718116
9235140718022
9264140627057
9277140721040
9276140731046

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 69284
Status: Resolved
Manufacturer: Aerogen Ltd.
Sold By: authorized medical distributors
Manufactured In: Ireland
Units Affected: 4 products (2,421 power adapters; 1,223 power adapters; 36 power adapters; 323 power adapters)
Distributed To: California, Georgia, Illinois, Mississippi, North Carolina, Texas

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response