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.

© 2026 Go Backs. All rights reserved.

Medium RiskFDA Drug
Medical Devices/Home Healthcare

Ferring Pharmaceuticals Inc: ZOMA-Jet Needle-Free Injector Pens Recalled for Breaking and Disintegrating

Agency Publication Date: March 30, 2021
Share:
Sign in to monitor this recall

Summary

Ferring Pharmaceuticals Inc. has recalled 1,870 ZOMA-Jet 5 and ZOMA-Jet 10 Demonstration Kits, which are needle-free delivery devices used with ZOMACTON (somatropin) for injection. The recall was initiated because the injector pens can break apart and disintegrate into pieces during use. This issue was identified following multiple customer complaints regarding the delivery system's structural integrity.

Risk

If the injector pen breaks or disintegrates during use, it may cause mechanical failure of the drug delivery system, potentially leading to incorrect dosing or injury from flying pieces of the device.

What You Should Do

  1. Check your device kit to see if it is a ZOMA-Jet 5 (UPC 3 55566 18031 5) or ZOMA-Jet 10 (UPC 3 55566 19031 4) Demonstration Kit.
  2. Verify the identifying numbers on your device packaging against the following affected codes for ZOMA-Jet 5: 201601320031, 201702320207, 201731220039, 201817120044, 201912720086, or 201912320044.
  3. Check your ZOMA-Jet 10 device for any of the 36 affected codes, including 201827020015, 201826020065, 201835320058, 201835320009, 201901820009, 201901420200, 201902120010, 201913720148, or 201912920021.
  4. Immediately stop using the demonstration kit if it matches the affected UPCs and codes listed above.
  5. Contact your healthcare provider or pharmacist for guidance regarding your medication delivery and to report any issues with the device.
  6. Return any unused or defective product to the place of purchase for a refund and contact Ferring Pharmaceuticals Inc. at 1-888-337-7464 for further instructions.
  7. Contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions or to report an injury.

Your Remedy Options

💰Full Refund

Healthcare provider consultation and pharmacy refund

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: ZOMA-Jet 5 Demonstration Kit, Needle-free delivery device for use with ZOMACTON (somatropin) for injection 5mg vial
Model:
D-0317-2021
UPC Codes:
355566180315
Lot Numbers:
201601320031
201702320207
201731220039
201817120044
201912720086
201912320044
Product: ZOMA-Jet 10 Demonstration Kit, Needle-free delivery device for use with ZOMACTON (somatropin) for injection 10 mg vial
Model:
D-0318-2021
UPC Codes:
355566190314
Lot Numbers:
201827020015
201826020065
201835320058
201835320009
201834920003
201835220007
201901820009
201901420200
201902120010
201901120019
201901420005
201901020180
201901520015
201900720001
201900920004
201904620003
201902120011
201904420007
201904520015
201904920002
201905020111
201904620004
201905720011
201907320003
201907320030
201907820007
201907420017
201910820009
201915620014
201910920016
201910620017
201910820020
201911320048
201911320095
201913720148
201912920021

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 87455
Status: Resolved
Manufacturer: Ferring Pharmaceuticals Inc
Sold By: Pharmacies; Healthcare providers
Manufactured In: United States
Units Affected: 2 products (301 devices; 1569 devices)
Distributed To: Nationwide

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 · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.