New Standard Device Inc Metalogix Slotted 90 Tubular Wrench x 10mm REF 900104 LOT A29618A Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Metalogix Slotted 90 Tubular Wrench x 10mm REF 900104 LOT A29618A
Brand
New Standard Device Inc
Lot Codes / Batch Numbers
Catalog/Part Number: 900104 UDI-DI (GTIN): 854641008112 Lot Number: A29618A
Products Sold
Catalog/Part Number: 900104 UDI-DI (GTIN): 854641008112 Lot Number: A29618A
New Standard Device Inc is recalling Metalogix Slotted 90 Tubular Wrench x 10mm REF 900104 LOT A29618A due to Due to manufacturing processing error, wrench causing stripping when torqueing nuts.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Due to manufacturing processing error, wrench causing stripping when torqueing nuts.
Recommended Action
Per FDA guidance
On 08/19/2019, the firm sent via email an "FIELD SAFETY NOTICE" informing customers that the Slotted 90 degree Tubular Wrench was stripping when torqueing nuts in the application process. Customers were asked to: -remove the affected products from inventory and return to Metalogix Inc. at 4848 Research Drive, San Antonio, TX 78240 ATTENTION: QA Dept.
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
AZ, CT, GA, OH, VA
Page updated: Jan 10, 2026