Blue Diamond Digital Inflation Device, REF: IN7152/C, IN7352/C, IN7403/C, IN7802/C, IN7852/C, IN7130/C
Class I - DangerousWhat Should You Do?
- 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).
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- 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.govFDA Recall Number: Z-0064-2025
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