Irvine Scientific Sales Co Inc Wallace Oocyte Recovery Needles,Oocyte Recovery sets, 750 mm tube with flushing connector, Product Number: KLN-750, and KLN-750. Retrieval of Oocytes. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Wallace Oocyte Recovery Needles,Oocyte Recovery sets, 750 mm tube with flushing connector, Product Number: KLN-750, and KLN-750. Retrieval of Oocytes.
Brand
Irvine Scientific Sales Co Inc
Lot Codes / Batch Numbers
Lot Number: 1270648, exp: 02/10/2013, 1281024, exp: 02/04/2013, and 1284914, exp: 03/11/2013.
Products Sold
Lot Number: 1270648, exp: 02/10/2013; 1281024, exp: 02/04/2013; and 1284914, exp: 03/11/2013.
Irvine Scientific Sales Co Inc is recalling Wallace Oocyte Recovery Needles,Oocyte Recovery sets, 750 mm tube with flushing connector, Product N due to Smiths Medical International became aware that certain lots of Wallace oocyte Recovery Sets have a damaged needle tip.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Smiths Medical International became aware that certain lots of Wallace oocyte Recovery Sets have a damaged needle tip.
Recommended Action
Per FDA guidance
The recall was initiated by Smiths Medical on October 22, 2008 with the forwarding a recall notification to Irvine Scientific. Smiths Medical International sells the products to Irvine Scientific for distribution in the U.S. Irvine Scientific is the U.S. Agent. Irvine Scientific issued an Urgent Field Safety Notice Letter, dated 10/22/2008, with attached fax-back Customer Response form to their customers via US Postal service beginning on October 24, 2008. Irvine Scientific requested their customers to complete an inventory summary on the Customer Response form and contact the firm to arrange for the return of any remaining product in their inventory to the firm.
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