DigitalDiagnost Release 3.1 (Stitching Patient Support) 712026
Class I - DangerousWhat Should You Do?
- Check if you have this product: Serial Numbers: SN14000256 SN14000250 SN15000024 SN14000170 SN14000052 SN14000224 SN15000039 SN14000144 SN14000253 SN14000239 SN14000186 SN14000075 SN14000193 SN14000254 SN15000001 SN14000089 SN14000223 SN14000267 SN14000238 SN14000164 SN14000165 SN14000200 SN14000005 SN14000040 SN15000015 SN15000029 SN14000120
- 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:
- Philips Medical Systems Gmbh, DMC
- Reason for Recall:
- The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
DigitalDiagnost Release 3.1 (Stitching Patient Support) 712026
Product Codes/Lot Numbers:
Serial Numbers: SN14000256 SN14000250 SN15000024 SN14000170 SN14000052 SN14000224 SN15000039 SN14000144 SN14000253 SN14000239 SN14000186 SN14000075 SN14000193 SN14000254 SN15000001 SN14000089 SN14000223 SN14000267 SN14000238 SN14000164 SN14000165 SN14000200 SN14000005 SN14000040 SN15000015 SN15000029 SN14000120
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-2862-2018
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