Southmedic Inc Po Box 1365 Barrie Canada Ontario Vapofils with Stainless Steel Block Ends, Item Number V0507F (Isoflurane). The vapofil is a keyed anesthetic transfer tube that transfers the anesthetic from the bottle to the vaporizer. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Vapofils with Stainless Steel Block Ends, Item Number V0507F (Isoflurane). The vapofil is a keyed anesthetic transfer tube that transfers the anesthetic from the bottle to the vaporizer.
Brand
Southmedic Inc Po Box 1365 Barrie Canada Ontario
Lot Codes / Batch Numbers
Lot numbers : I02156, I07205, I03096, I02286, & I12095
Products Sold
Lot numbers : I02156, I07205, I03096, I02286, & I12095
Southmedic Inc Po Box 1365 Barrie Canada Ontario is recalling Vapofils with Stainless Steel Block Ends, Item Number V0507F (Isoflurane). The vapofil is a keyed due to Southmedic has initiated this recall because their Japanese distributor received field reports of leaking vapofils. Leakage may cause non-toxic spills. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Southmedic has initiated this recall because their Japanese distributor received field reports of leaking vapofils. Leakage may cause non-toxic spills in the hospital environment, distraction of practitioners during conduct of anesthesia and surgery, and may damage certain plastic equipment. Leakage may also expose patients to low concentrations of volatile anesthetics.
Recommended Action
Per FDA guidance
Recall letters were sent to both US consignees via US Postal Service delivery with signature receipt required on April 21, 2006. Each letter included a Recall and Effectiveness Check Form for each consignee to fill out and fax to Southmedic. U.S. and international consignees were instructed to examine inventory immediately to identify if they have any product on hand, discontinue the distribution of these products and return all affected products to Southmedic. Consignees were also instructed to immediately notify their customers if they have further distributed these products.
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 noticeDistribution
As reported by FDA
FL, IN, NJ
Page updated: Jan 10, 2026