Lower riskMedical device recall · FDA · Published August 14, 2019
New Standard Device Metalogix Slotted Wrench Recall: Stripping Nuts Hazard
New Standard Device recalls 10mm slotted tubular wrenches with lot A29618A due to stripping nuts during use. Affected units may cause damage to fasteners.
“New Standard Device Metalogix Slotted Wrench Recall: Stripping Nuts Hazard.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/67223-new-standard-device-metalogix-slotted-wrench-recall-stripping-nuts-hazard. Based on FDA recall #Z-1280-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1280-2022%22&limit=1).
The FDA announced on Aug. 14, 2019, that New Standard Device Inc voluntarily recalled Metalogix Slotted 90 Tubular Wrench x 10mm REF 900104 LOT A29618A due to a manufacturing error causing wrench stripping when torqueing nuts.
How to tell if you have it
Brand: New Standard Device
Product: Metalogix Slotted 90 Tubular Wrench x 10mm
REF: 900104
Lot Number: A29618A
Catalog/Part Number: 900104
UDI-DI (GTIN): 854641008112
Quantity: 14 devices
Distribution: U.S. states AZ, CT, GA, OH, VA
The hazard
According to the FDA, a manufacturing processing error causes the wrench to strip when torqueing nuts.
Context
GovInfoNow's records show New Standard Device Inc has three other recalls on record since July 23, 2019. Other recent recalls of similar products include Synthes 2.4V Tap Locking Screw Tap Recall (Feb. 25, 2026), Olympus HX-400U-30 Ligating Device Recall (Oct. 30, 2025), and Philips Spectral CT 7500 on Rails Recall (Jan. 7, 2026).
How to tell if you have this one
Check for the model number 900104 and lot number A29618A on the wrench. The product was sold with the reference code REF 900104.
Brand
New Standard Device
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Details
Look for model number 900104 and lot number A29618A on the wrench.
Where it went and when
Where it was distributed
Distributed in 5 states.
Listed by the agency
Not listed
FDA distribution: “U.S.: AZ. CT, GA, OH, and VA O.U.S.: N/A” States read from FDA’s own wording; “not listed” means the notice does not name it.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-1280-2022 (August 14, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1280-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.