Hollister CalciCare Calcium Alginate Dressing REF 529937R calcium alginate dressings are indicated for moderate to heavily exuding chronic and acute wounds such as: ¿ pressure ulcers ¿ leg ulcers ¿ cavity wounds ¿ lacerations ¿ post-operative surgical wounds
Class I - DangerousWhat Should You Do?
- Check if you have this product: Model Number: 529937R UDI-DI code: 0060075029530 Lot Number: W00070134
- 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:
- Advanced Medical Solutions Ltd.
- Reason for Recall:
- Due to defects on primary packaging pouch that compromise the device's ability to maintain a sterile barrier.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
Hollister CalciCare Calcium Alginate Dressing REF 529937R calcium alginate dressings are indicated for moderate to heavily exuding chronic and acute wounds such as: ¿ pressure ulcers ¿ leg ulcers ¿ cavity wounds ¿ lacerations ¿ post-operative surgical wounds
Product Codes/Lot Numbers:
Model Number: 529937R UDI-DI code: 0060075029530 Lot Number: W00070134
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0617-2025
Related Recalls
Due to defects on primary packaging pouch that compromise the device's ability to maintain a sterile barrier.
McKesson Calcium Alginate Dressing MFR# 3562 Wound dressing indicated for moderate to heavily exuding chronic and acute wounds, and to control minor bleeding in superficial wounds.
Advanced Medical Solutions
Due to defects on primary packaging pouch that compromise the device's ability to maintain a sterile barrier.
On 08 January 2015 AMS Sole Customer for the products notified AMS of the issue after discovering the misplaced IFUs during its review of packaging in its warehouse