Applied Medical Resources Corp 22872 Avenida Empresa # 3 Rancho Santa Applied Blunt Tip Trocar Models C0717 and C0718 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Applied Blunt Tip Trocar Models C0717 and C0718
Brand
Applied Medical Resources Corp 22872 Avenida Empresa # 3 Rancho Santa
Lot Codes / Batch Numbers
45208001001 to 452084001008 containing 1 each of lot 127322=8 each, 452451005001 to 452451005003 containing 1 each of lot 127322=3 each, 453029001001 to 453029001017 containing 1 each of lot 127322 = 17 each, 453715004002 containing 1 each of lot 126803 = 1 each, 454116005001 to 454116005002 containing 1 each of lot 127322 = 2, 454608003001 to 454608003006 containing 1 each of lot 172528 = 6 each.
Products Sold
Trocars are assembled into procedure kits. Trocars have thier own serial number but the kit lots are relevant and include: 45036301001 to 45036301007 containing 1 each of lot 126803 = 71 each; 45208001001 to 452084001008 containing 1 each of lot 127322=8 each; 452451005001 to 452451005003 containing 1 each of lot 127322=3 each; 453029001001 to 453029001017 containing 1 each of lot 127322 = 17 each; 453715004002 containing 1 each of lot 126803 = 1 each; 454116005001 to 454116005002 containing 1 each of lot 127322 = 2; 454608003001 to 454608003006 containing 1 each of lot 172528 = 6 each.
Applied Medical Resources Corp 22872 Avenida Empresa # 3 Rancho Santa is recalling Applied Blunt Tip Trocar Models C0717 and C0718 due to Inadequate trocar tip assembly that might yeild parts to patients.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Inadequate trocar tip assembly that might yeild parts to patients.
Recommended Action
Per FDA guidance
Initiated recall by letter on 9/16/2004 via Fedex/UPS. Follow-up to nonresponders in 30 days.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026