basixTOUCH Inflation Device, REF: IN8130/JPC, IN8152/C, IN8302/C, IN8352/C, IN8802/C, IN8130/C, IN8130/C
Class I - DangerousWhat Should You Do?
- Check if you have this product: REF/UDI-DI/Lot(Expiration): IN8130/JPC/00884450621073/H2929530(4/29/2027). IN8152/C/00884450621301/H2925219(4/22/2027), H2929412(4/29/2027), H2938005(5/12/2027), H2938006(5/12/2027), H2943498(5/19/2027), H2943499(5/19/2027), H2972593(5/26/2027), H2972594(5/26/2027), H2978092(6/3/2027). IN8302/C/00884450621325/H2925221(4/22/2027). IN8352/C/00884450621349/H2934719(5/5/2027). IN8802/C/00884450621417/H2925222(4/22/2027), H2934720(5/12/2027), H2943517(5/19/2027), H2972598(5/26/2027). IN8130/C/00884450621059/H2925215(4/22/2027), H2929410(4/29/2027), H2934714(5/5/2027), H2937998(5/12/2027), H2938000(5/12/2027), H2943487(5/19/2027). IN8130/C/00884450621059/H2972590(5/26/2027), H2978089(6/3/2027), H2978090(6/3/2027), H2978091(6/3/2027), H2989571(6/17/2027).
- 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:
basixTOUCH Inflation Device, REF: IN8130/JPC, IN8152/C, IN8302/C, IN8352/C, IN8802/C, IN8130/C, IN8130/C
Product Codes/Lot Numbers:
REF/UDI-DI/Lot(Expiration): IN8130/JPC/00884450621073/H2929530(4/29/2027). IN8152/C/00884450621301/H2925219(4/22/2027), H2929412(4/29/2027), H2938005(5/12/2027), H2938006(5/12/2027), H2943498(5/19/2027), H2943499(5/19/2027), H2972593(5/26/2027), H2972594(5/26/2027), H2978092(6/3/2027). IN8302/C/00884450621325/H2925221(4/22/2027). IN8352/C/00884450621349/H2934719(5/5/2027). IN8802/C/00884450621417/H2925222(4/22/2027), H2934720(5/12/2027), H2943517(5/19/2027), H2972598(5/26/2027). IN8130/C/00884450621059/H2925215(4/22/2027), H2929410(4/29/2027), H2934714(5/5/2027), H2937998(5/12/2027), H2938000(5/12/2027), H2943487(5/19/2027). IN8130/C/00884450621059/H2972590(5/26/2027), H2978089(6/3/2027), H2978090(6/3/2027), H2978091(6/3/2027), H2989571(6/17/2027).
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0072-2025
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