Device recalls

Straumann Bone Level Tapered (BLT) Implant, D 4.1mm RC, SLActive 14mm, Roxolid, Loxim (Article 021.5314); implant, endosseous, root-form

Straumann USA LLC · Bone Level Tapered (BLT) Implant, D 4.1mm RC, SLActive 14mm, Roxolid, Loxim may inadvertently contain implants that are 12mm in length instead of 14mm as the l…

Open, ClassifiedUnder Investigation by firmZ-2935-2026
Open FDA's page for this record
Cfres ID
221565
Product res number
Z-2935-2026
Event date initiated
2026-07-16
Event date posted
2026-08-11
Recall status
Open, Classified
Res event number
99441
Product code
DZE
Product description
Straumann Bone Level Tapered (BLT) Implant, D 4.1mm RC, SLActive 14mm, Roxolid, Loxim (Article 021.5314); implant, endosseous, root-form
Code info
UDI/DI 7630031707055, Lot ZVFV5
Firm FEI number
1000121052
Recalling firm
Straumann USA LLC
Address 1
60 Minuteman Rd
City
Andover
State
MA
Postal code
01810-1008
Additional info contact
Todd Shevlin 978-759-5442
Root cause description
Under Investigation by firm
Product quantity
175 units
Distribution pattern
US Nationwide distribution.
Reason for recall

Bone Level Tapered (BLT) Implant, D 4.1mm RC, SLActive 14mm, Roxolid, Loxim may inadvertently contain implants that are 12mm in length instead of 14mm as the labeling would suggest.

Action

Straumann Group issued an Urgent Field Safety Action notice to its consignees on 7/16/2026 via UPS. The notice explained the issue, potential risk, and requested the following: "Action to be taken: 1. Identify and segregate any units in your stock with carton packaging labelled as Article 021.5314 Bone Level Tapered Implant, D 4.1mm RC, SLActive 14mm, Roxolid, Loxim" (Article 021.5314, Lot ZVFV5) 2. Return any segregated units with carton packaging labelled as Article 021.5314 Bone Level Tapered Implant, D 4.1mm RC, SLActive 14mm, Roxolid, Loxim", Lot ZVFV5 for replacement or refund 3. If the product has been implanted with no unexpected clinical occurrence during implantation, then no special follow up outside of the dentist s standard follow procedure is necessary 4. In all cases, complete and return the enclosed Customer Confirmation Form with the affected product using the return UPS label provided to: Straumann USA, LLC 60 Minuteman Road Andover, MA 01810 If product is not being returned, the completed Customer Confirmation Form can be scanned and emailed to todd.shevlin@straumann.com Transmission of the Field Safety Notice This notice needs to be passed on to all those who need to be aware within your organization or to any organization where the affected devices have been transferred."

K numbers
K140878
Harmonized identifiers (openFDA)
Device name
Implant, Endosseous, Root-Form
Medical specialty description
Dental
Regulation number
872.3640
Device class
2
K number
K020617, K900793, K162853, K191895, K091051, K133327, K974358, K953280, K960026, K983742, K952120, K051507, K130221, K964330, K080713, K151391, K063874, K811923, K191201, K070570, K232740, K173975, K160581, K034022, K953000, K071070, K024044, K772304, K902968, K130787, K120043, K914764, K223697, K952917, K963945, K031475, K891617, K140202, K170031, K040946 +1,509 more
PMA number
P800035, P860012
Registration number
3011936113, 3001082453, 2023623, 2245590, 3004201263, 3013111692, 2029275, 3006405073, 2032098, 3007518363, 3006592743, 3025517712, 3015775866, 3004049923, 8020776, 9613283, 9611993, 3011587077, 3015160953, 1424785, 3031462380, 3038549074, 2024024, 3008088588, 3014596751, 3011656326, 9680605, 2031884, 8030870, 8010591, 9611992, 2921595, 3005216725, 3024859204, 3008252900, 3009528826, 3011103459, 3009611645, 3011187779, 2183744 +288 more
FEI number
3011936113, 3001082453, 2023623, 3002807692, 2245590, 3004201263, 3013111692, 3006405073, 3007518363, 3006592743, 3025517712, 3015775866, 3003110073, 3004049923, 3002806651, 3011587077, 3003267134, 3015160953, 1000306551, 3031462380, 3038549074, 3000215273, 2024024, 3008088588, 3014596751, 3011656326, 5870, 2921595, 3005216725, 3002807009, 3024859204, 3002806577, 3008252900, 3009528826, 3011103459, 3003054571, 3009611645, 3011187779, 4224, 2183744 +288 more
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.