DigitalDiagnost, Single-Detect (Stitching Patient Support) 712062
Class I - DangerousWhat Should You Do?
- Check if you have this product: Serial Numbers: 386786/SN0702512 375366 416255/SN0902004 358322 388667/SN0802105 375367 397229/SN0802250 396838/SN0802365 386108/SN0802044 405687/SN0802469 354125 362438 406156/SN0802537 413697/SN0802634 402853/SN0902012 405889/SN0802629 383385/SN0802011 378827/SN0802021 384013/SN0702495 358017 358496 377925/SN0802060 356953 355621 357888 356956 368431 356963 406016/SN0802476 346522 375370 70700 351321 392504/SN0802182
- 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, Single-Detect (Stitching Patient Support) 712062
Product Codes/Lot Numbers:
Serial Numbers: 386786/SN0702512 375366 416255/SN0902004 358322 388667/SN0802105 375367 397229/SN0802250 396838/SN0802365 386108/SN0802044 405687/SN0802469 354125 362438 406156/SN0802537 413697/SN0802634 402853/SN0902012 405889/SN0802629 383385/SN0802011 378827/SN0802021 384013/SN0702495 358017 358496 377925/SN0802060 356953 355621 357888 356956 368431 356963 406016/SN0802476 346522 375370 70700 351321 392504/SN0802182
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-2866-2018
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