🔍 RecallPedia

Blue Diamond Digital Inflation Device, REF: IN7152/C, IN7352/C, IN7403/C, IN7802/C, IN7852/C, IN7130/C

Class I - Dangerous
🏥 Medical Devices Recalled: August 19, 2024 Merit Medical Systems Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    REF/UDI-DI/Lot(Expiration): IN7152/C/00884450381168/H2918432(4/15/2027), H2925197(4/22/2027), H2929406(4/29/2027), H2929407(4/29/2027, H2934708(5/5/2027), H2937991(6/3/2027), H2937992(5/19/2027), H2943482(5/19/2027), H2972588(6/3/2027), H2972589(5/26/2027).: . IN7352/C/00884450409879/H2934710(5/5/2027). IN7403/C/00884450409886/H2943483(4/30/2027). IN7802/C/00884450498743/H2918435(4/22/2027), H2929409(4/29/2027), H2934711(5/5/2027), H2937995(5/12/2027), H2943485(5/19/2027), H2978087(6/3/2027). IN7852/C/00884450498750/H2937355(9/30/2025). IN7130/C/00884450409855/H2918431(4/15/2027), H2925196(4/22/2027), H2934706(5/5/2027), H2937988(6/3/2027), H2943481(5/19/2027), H2972587(5/26/2027), H2978086(6/3/2027).
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Merit Medical Systems, Inc.
Reason for Recall:
Inflation devices may have a small hole in the sterile barrier of the device and use of affected devices may result in exposure to pathogens/pyrogens which could lead to infection.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

Blue Diamond Digital Inflation Device, REF: IN7152/C, IN7352/C, IN7403/C, IN7802/C, IN7852/C, IN7130/C

Product Codes/Lot Numbers:

REF/UDI-DI/Lot(Expiration): IN7152/C/00884450381168/H2918432(4/15/2027), H2925197(4/22/2027), H2929406(4/29/2027), H2929407(4/29/2027, H2934708(5/5/2027), H2937991(6/3/2027), H2937992(5/19/2027), H2943482(5/19/2027), H2972588(6/3/2027), H2972589(5/26/2027).: . IN7352/C/00884450409879/H2934710(5/5/2027). IN7403/C/00884450409886/H2943483(4/30/2027). IN7802/C/00884450498743/H2918435(4/22/2027), H2929409(4/29/2027), H2934711(5/5/2027), H2937995(5/12/2027), H2943485(5/19/2027), H2978087(6/3/2027). IN7852/C/00884450498750/H2937355(9/30/2025). IN7130/C/00884450409855/H2918431(4/15/2027), H2925196(4/22/2027), H2934706(5/5/2027), H2937988(6/3/2027), H2943481(5/19/2027), H2972587(5/26/2027), H2978086(6/3/2027).

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0064-2025

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