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Stop using now Drug recall · FDA · Published March 11, 2021

Ferring Recalls ZOMA-Jet 10 Kits Due to Defective Delivery System

Ferring Pharmaceuticals recalls 1,569 ZOMA-Jet 10 Demonstration Kits because the device may break apart. Check lot numbers and UPC.

🇺🇸 FDA recall #D-0318-2021DrugFerring Pharmaceuticals ›
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Recalling firmFerring Pharmaceuticals Inc100 Interpace Pkwy · Parsippany, NJ 07054-1149
✎ GovInfoNow plain-language explainer

Ferring Pharmaceuticals Inc is recalling the ZOMA-Jet 10 Demonstration Kit, a needle-free delivery device intended for use with ZOMACTON injections. The recall was initiated due to customer complaints that the injector pen can break apart and disintegrate into pieces during use. This defect poses a risk of injury or improper medication delivery. Read more at govinfonow.com/recall/36479-ferring-recalls-zoma-jet-10-kits-due-to-defective-delivery.

Source Summary by GovInfoNow · govinfonow.com/recall/36479-ferring-recalls-zoma-jet-10-kits-due-to-defective-delivery · Updated October 11, 2026 · FDA enforcement record: FDA #D-0318-2021

Cite this page

“Ferring Recalls ZOMA-Jet 10 Kits Due to Defective Delivery System.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/36479-ferring-recalls-zoma-jet-10-kits-due-to-defective-delivery. Based on FDA recall #D-0318-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0318-2021%22&limit=1).

The FDA announced on March 11, 2021, that Ferring Pharmaceuticals Inc. is recalling the ZOMA-Jet 10 Demonstration Kit due to a defective delivery system. The agency said customers reported the injector pen breaking apart and disintegrating into pieces.

How to tell if you have it

  • ZOMA-Jet 10 Demonstration Kit
  • Needle-free delivery device for use with ZOMACTON (somatropin) for injection 10 mg vial
  • UPC 3 55566 19031 4
  • Lot codes: 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

The hazard

The recall involves a defective delivery system where customer complaints concern the injector pen breaking apart and disintegrating into pieces. The FDA said these issues were reported by customers.

Context

GovInfoNow's records show Ferring Pharmaceuticals Inc has had 8 other recalls on record since August 23, 2012. Other recent recalls of similar products include Ferring Endometrin Vaginal Inserts Recall (June 12, 2023), Ferring Menopur 75 IU Recall (March 2, 2021), and Ferring DDAVP Nasal Spray Recall (July 21, 2020). Other recent recalls of similar products include Ajanta Pharma Fenofibrate Capsules Recall (May 28, 2026), Shoolin Pharma Chem Sildenafil Recall (August 3, 2026), and ANI Pharmaceuticals Recalls Estradiol Gel Due to Defective Containers (May 12, 2026).

How to tell if you have this one

Look for the ZOMA-Jet 10 Demonstration Kit, which includes a ZOMA-Jet 10 device, 7 Needle-Free Heads, a carrying case, and a user manual. Check the UPC (3 55566 19031 4) and the lot numbers listed in the record, such as 201827020015 or 201907820007.

  • Brand
    Ferring Pharmaceuticals
  • Product
    ZOMA-Jet 10 Demonstration Kit, Needle-free delivery device for use with ZOMACTON (somatropin) for injection 10 mg vial
  • Category
    Drug
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Terminated
  • Distribution
    Nationwide in the USA
Recall numberProduct, codes & lotsQuantity
D-0317-2021ZOMA-Jet 5 Demonstration Kit, Needle-free delivery device for use with ZOMACTON (somatropin) for injection 5mg vial, Rx only, ZOMA-Jet 5 Demonstration Kit contains -ZOMA-Jet 5 device - 5 Needle-Free Head A's - 2 Vial Adaptors - 1 Carrying Case - 1 User Manual; Manufactured for: Ferring Pharmaceuticals Inc. Parsippany, NJ 07054; UPC 3 55566 18031 5.; 201601320031 201702320207 201731220039 201817120044 201912720086 201912320044301 devices
D-0318-2021ZOMA-Jet 10 Demonstration Kit, Needle-free delivery device for use with ZOMACTON (somatropin) for injection 10 mg vial, ZOMA-Jet 10 Demonstration Kit contains -ZOMA-Jet 10 device - 7 Needle-Free Head A's - 1 Carrying Case - 1 User Manual; Manufactured for: Ferring Pharmaceuticals Inc. Parsippany, NJ 07054; UPC 3 55566 19031 4.; 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 2019129200211569 devices
Based on the official FDA remedy

What to do — step by step

  1. Stop using the device

    Do not use the ZOMA-Jet 10 Demonstration Kit further due to the risk of it breaking apart.

  2. Check your lot number

    Verify if your kit's lot number matches one of the recalled lots, such as 201904620003 or 201915620014.

  3. Contact the manufacturer

    Reach out to Ferring Pharmaceuticals Inc for further instructions on how to handle the recalled kit.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide in the USA” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 2.2 years after the firm started it.

1. Firm started the recall: Mar 11, 202112. FDA classified it Class II: Mar 30, 202123. Published in FDA’s Enforcement Report: Apr 7, 202134. FDA terminated the recall: Jun 7, 2023420212023
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

Who is manufacturing this recalled product?

The product was manufactured for Ferring Pharmaceuticals Inc, located in Parsippany, NJ.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #D-0318-2021 (March 11, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0318-2021 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA