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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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Medium RiskFDA Device
Medical Devices/Diagnostic Equipment

MEDLINE INDUSTRIES, LP - Northfield: Adult Blood and Blood Culture Kits Recalled for Possible Expired Components

Agency Publication Date: February 1, 2024
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Summary

Medline Industries, LP has recalled 26,715 Adult Blood and Blood Culture Kits because some kits contain a Bactec component with an expiration date that does not match the information on the kit's outer insert. If a medical professional relies on the kit insert rather than checking the bottle itself, they may inadvertently use an expired component during blood collection or testing. These kits were distributed nationwide across the United States between December 2023 and early 2024.

Risk

Using an expired Bactec component can lead to inaccurate blood culture results, potentially causing delayed or incorrect treatment for serious infections. While no injuries have been reported, the risk remains that the chemical integrity of the component may be compromised after its true expiration date.

What You Should Do

  1. Locate your Medline Blood Culture Kit and check the reorder number on the outer packaging. Affected reorder numbers include DYNDH1694A, DYNDH1738A, DYNDH1714A, DYNDH1626B, DYNDH1723, DYNDH1622C, and DYNDH1194A.
  2. If the reorder number matches, check the Lot Number on the case or unit. Specifically look for lots: 23JBH262, 23JBC264, 23JBM366, 23KBC138, 23KBH642, 23JBO541, 23JBQ525, or 23JBO540.
  3. Verify the individual Bactec bottle inside the kit; do not rely on the expiration date printed on the kit's paper insert. Inspect the bottle itself for the manufacturer's printed expiration date.
  4. If you identify an affected kit with an expired internal component, stop using it immediately and set it aside for return or disposal as instructed by the manufacturer.
  5. Contact Medline Industries, LP or your healthcare provider for further instructions on returning affected units and obtaining potential replacements or refunds.
  6. For additional questions, contact the FDA at 1-888-463-6332 (1-888-INFO-FDA) or visit www.fda.gov/medical-devices/medical-device-recalls.

Your Remedy Options

๐Ÿ“‹Other Action

Contact healthcare provider or manufacturer for instructions.

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

Affected Products

Product: MEDLINE ADULT BLOOD CULTURE KIT
Model / REF:
DYNDH1694A
UPC Codes:
40195327139958
10195327139957
Lot Numbers:
23JBH262
23JBC264
Product: MEDLINE BLOOD CULTURE BOTTLE KIT
Model / REF:
DYNDH1738A
UPC Codes:
40195327239849
10195327239848
Lot Numbers:
23JBM366
Product: MEDLINE BLOOD CULTURE COLLECTION KIT
Model / REF:
DYNDH1714A
UPC Codes:
40195327347551
10195327347550
Lot Numbers:
23KBC138
Product: MEDLINE BLOOD CULTURE COLLECTION KIT
Model / REF:
DYNDH1626B
UPC Codes:
40195327323333
10195327323332
Lot Numbers:
23KBH642
Product: MEDLINE BLOOD CULTURE KIT
Model / REF:
DYNDH1723
UPC Codes:
40195327134205
10195327134204
Lot Numbers:
23JBO541
Product: MEDLINE BLOOD CULTURE KIT
Model / REF:
DYNDH1622C
UPC Codes:
40195327509874
10195327509873
Lot Numbers:
23JBQ525
Product: MEDLINE BLOOD CULTURE TRAY ADULT
Model / REF:
DYNDH1194A
UPC Codes:
40195327432301
10195327432300
Lot Numbers:
23JBO540

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 93731
Status: Active
Manufacturer: MEDLINE INDUSTRIES, LP - Northfield
Sold By: Medline Industries, LP
Manufactured In: United States
Units Affected: 7 products (13860 units; 775 units; 4320 units; 500 units; 960 units; 4200 units; 2100 units)
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 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.