Recall StatusTerminated
Date Initiated2020-01-15
Date Terminated2023-03-17
Product Quantity343105 total
Reason for Recall
There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
Firm Action
An Urgent Medical Device Recall notification letter dated 1/15/20 was sent to customers.
Our records indicate you have received products that are subject to this field action. We are now notifying our customers to take the following actions:
1. If you have affected stock, immediately identify product, discontinue use and quarantine any products with the product codes and lot numbers listed above.
2. To acknowledge receipt of this Urgent Medical Device Recall Notice or to return product, complete the enclosed Recall Acknowledgement Form and fax it to 1-855-419-8507, Attn: Customer Service or email to
[email protected]. This will allow us to document the amount of product you have on hand for return. A customer service representative will contact you with a Return Goods Authorization (RGA) Number and will provide instructions for the return of products to Teleflex Medical.
3. If you have no affected stock, please complete the enclosed Recall Acknowledgment Form and fax it to 1-855-419-8507, Attn: Customer Service or email to
[email protected]. This will allow us to document your receipt of this letter.
Distribution Pattern
The products were distributed to the following US states: AK, AR, AZ, CA, CO, CT, FL, GA, ID, IL, IN, LA, MA, MD, MI, MN, MO, MT, NC, NE, NH, NJ, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, and WY.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.