LARGE CANNULATED SCREWS 71107105Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03596010291295), received between Dec 20, 2017 and Dec 20, 2017 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryDec 20, 2017Insufficient Device Problem Information; Insufficient Device Problem Information

  IT WAS REPORTED THAT PATIENT DEVELOPED A SKIN PROBLEM IN THE HOSPITAL AFTER SURGERY. PATIENT HAS BEEN PRESCRIBED ANYTHING FROM ANTIBIOTICS TO ANTIHISTAMINES. THE LAST DOCTOR SUGGESTED A SKIN TEST TO WHICH CAME IN POSITIVE FOR GOLD SODIUM THIOSULFATE. PATIENT NOW NEEDS TO GET FURTHER METAL TESTS TO DETERMINE TO WHICH OTHER METAL HE MIGHT BE ALLERGIC SO THAT HE CAN GET TREATMENT. SYMPTOMS: HUGE RED SPOTS WITH ITCHING ALL OVER THE BODY AND SCALP. THEY SEEM TO BE GETTING WORSE. HE HAS UNDERGONE A SKIN SCRAPE TEST, HAS BEEN DIAGNOSED WITH (POSSIBLE) THINGS LIKE SCABIES, SKIN PSORIASIS, ECZEMA, SEASONAL ALLERGIES, ATOPIC DERMATITIS, ETC. JUST GRASPING FOR STRAWS.

  Patient problems: Reaction

  MAUDE report 7134512 ↗