Medical convenience kits Item Number/Description ANCV78BC HEART PACK - 205947 HGCV05K CV SET UP PACK MHPP97AR PACEMAKER PACK- 206010 UDBH37AW BASIC HEART PACK - 206044 UHPP82AH PERIPHERAL PACK - 209533 UICD62AN CARDIOVASCUALR SUPPLY (PS 907285) UICT16F CARDIO THORACIC DRAPE PACK (PS 907284) UIVA75I VASCULAR PACK

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    ANCV78BB UDI-DI 191072214362 Lot 8133811 Bag serial number 68273380; ANCV78BC UDI-DI 191072235169 Lot 8499811 Bag serial numbers N/A; HGCV05K UDI-DI 191072212474 Lot 8021411 Bag serial number 68154464; MHPP97AR UDI-DI 191072237446 Lot 8527511 Bag serial number N/A; UDBH37AW UDI-DI 191072235299 Lot 8194311 Bag serial numbers 68198334 68198335; UHPP82AH UDI-DI 191072216434 Lot 8112811 Bag serial number N/A; UICD62AN UDI-DI 191072200495 Lot 7999011 Bag serial number N/A; UICT16F UDI-DI 191072150431 Lot 8000411 Bag serial number N/A Lot 8331311 Bag serial number 17627819 Lot 8429011 Bag serial number 17749736; UIVA75I UDI-DI 191072229052 Lot 8056011 Bag serial number N/A; UIVA75J UDI-DI 191072235602 Lot 8422011 Bag serial number 68667536 * If Bag serial number is "n/a", then all of that lot is affected
  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:
American Contract Systems Inc.
Reason for Recall:
Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection process. These products have not been validated for exposure to multiple sterilization cycles. Therefore, product quality, safety, and effectiveness cannot be confirmed for product that was re-gassed.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

Medical convenience kits Item Number/Description ANCV78BC HEART PACK - 205947 HGCV05K CV SET UP PACK MHPP97AR PACEMAKER PACK- 206010 UDBH37AW BASIC HEART PACK - 206044 UHPP82AH PERIPHERAL PACK - 209533 UICD62AN CARDIOVASCUALR SUPPLY (PS 907285) UICT16F CARDIO THORACIC DRAPE PACK (PS 907284) UIVA75I VASCULAR PACK

Product Codes/Lot Numbers:

ANCV78BB UDI-DI 191072214362 Lot 8133811 Bag serial number 68273380; ANCV78BC UDI-DI 191072235169 Lot 8499811 Bag serial numbers N/A; HGCV05K UDI-DI 191072212474 Lot 8021411 Bag serial number 68154464; MHPP97AR UDI-DI 191072237446 Lot 8527511 Bag serial number N/A; UDBH37AW UDI-DI 191072235299 Lot 8194311 Bag serial numbers 68198334 68198335; UHPP82AH UDI-DI 191072216434 Lot 8112811 Bag serial number N/A; UICD62AN UDI-DI 191072200495 Lot 7999011 Bag serial number N/A; UICT16F UDI-DI 191072150431 Lot 8000411 Bag serial number N/A Lot 8331311 Bag serial number 17627819 Lot 8429011 Bag serial number 17749736; UIVA75I UDI-DI 191072229052 Lot 8056011 Bag serial number N/A; UIVA75J UDI-DI 191072235602 Lot 8422011 Bag serial number 68667536 * If Bag serial number is "n/a", then all of that lot is affected

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0176-2026

Related Recalls

Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection process. These products have not been validated for exposure to multiple sterilization cycles. Therefore, product quality, safety, and effectiveness cannot be confirmed for product that was re-gassed.

Sep 4, 2025 Other Medical Devices Nationwide View Details →

Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection process. These products have not been validated for exposure to multiple sterilization cycles. Therefore, product quality, safety, and effectiveness cannot be confirmed for product that was re-gassed.

Sep 4, 2025 Infusion Pumps Nationwide View Details →

Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection process. These products have not been validated for exposure to multiple sterilization cycles. Therefore, product quality, safety, and effectiveness cannot be confirmed for product that was re-gassed.

Sep 4, 2025 Other Medical Devices Nationwide View Details →