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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.

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Critical RiskFDA Drug
Medications & Supplements/Prescription Drugs

UDENYCA Injection Recalled for Temperature Abuse

Agency Publication Date: February 10, 2026
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Summary

McKesson is recalling 116 cartons of UDENYCA (pegfilgrastim-cbqv) injection, 6 mg/0.6mL Single Dose Prefilled Syringes. These specific units were stored incorrectly at room temperature instead of the required refrigerated environment, which can affect the medication's safety and effectiveness. The recall affects a specific subset of serial numbers from Lot 2199821 with an expiration date of May 31, 2027.

Risk

Storage of this medication outside of the required refrigerated temperature range can cause the drug to degrade, potentially making the treatment less effective for patients relying on it to help prevent infections during chemotherapy.

What You Should Do

  1. Check the serial number on your UDENYCA carton to see if it matches one of the 116 affected units. See the Affected Products section below for the full list of affected codes.
  2. If you have health concerns, contact your healthcare provider or pharmacist.
  3. Return any unused product to the place of purchase for a refund, throw it away, or contact McKesson for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for more information.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: UDENYCA, pegfilgrastim-cbqv injection, 6 mg/0.6mL Single Dose Prefilled Syringe
Variants: 6 mg/0.6mL, Single Dose Prefilled Syringe, Rx only
Serial Numbers (116):
160R694TT06X
1C74A686RPPG
1W6A2M777N3V
20825394KR8P
242E2RK3EA92
2DG49VH89EPG
2WEA2ADK1P4H
3KR2TVAG3VDH
42M0V0G9PM84
46E9XKDPTH1R
4AM12WEAE48H
4FGHR096DMNV
4MWGWM991XNA
4NEW8XD9DNM2
4Y2PYDFN9YA1
61EPX42R4K2A
63FN9VW5CAV7
69TG160DW2CV
69XFP3TMTP7X
6AWVDCNHTV61
6CEFY72W5GPA
6FHF1A59X0X4
6GA64FNDVGXY
6NW5FACPPWDW
75V19CF2A0PA
7HK7155YNAK3
7R51VVA1WX9T
7XCKXMH2EERC
85D8MFVM66D4
8F3Y5NFFHC64
8RDWKPM53N5R
8W1PVXC5NAFW
9338DPED7P3R
9A4CXFTGCPYN
9FKN5NRDX99A
9G79AR0RGAY4
9K28G80GGYXN
9NN7NXE40M13
A48PXEPE77YE
A8M168K58G64
AMR0RNWHTWMW
AR145NW8WTVX
AY19W6DEGRX4
C276HMDGRE49
CAY0ARAEGMCF
CKT370X2G4NP
D0DFAXCN6G5W
D54TXR8AD9Y8
DAK3XP1P3DMP
DH44AGKTX27F
Lot Numbers:
2199821 (Exp 05/31/2027)
NDC:
69448-025-63

Recall #: D-0353-2026. Only a subset of 116 cartons from Lot 2199821 are affected based on specific serial numbers.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98366
Status: Active
Manufacturer: McKesson
Sold By: Retail Pharmacies
Manufactured In: United States
Units Affected: 116 cartons
Distributed To: Nationwide
Agency Last Updated: February 26, 2026

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

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.