State

Northern Mariana Islands product recalls

73,503 recalls have nationwide distribution and so reach Northern Mariana Islands. 23 additional recalls listed Northern Mariana Islands specifically in their distribution scope.

What the numbers show

Total: 23
Critical: 0
Severe: 18
Most recent: 2026-09-23

Of the 23 recalls naming Northern Mariana Islands we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 18 (78%) are Severe.

Which agencies issued them

These figures cover only the 23 recalls whose distribution notice names Northern Mariana Islands specifically. The 73,503 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24601–24625 of 73526

HighFDA (Devices)·Z-1780-2021·2021-06-09
Tranberg MR Cannula: Inadequate Sterilization May Compromise Safety
CLINICAL LASERTHERMIA SYSTEMS AB is recalling the Tranberg MR Cannula due to potentially inadequate sterilization of certain lots. Affected units were distributed to medical facilities in the US and internationally.
Product
Tranberg MR Cannula, REF: 4013-05, Rx Only, Sterile EO - Product Usage: used with the Tranberg¿ MR Introducer; a device used to aid the insertion of the Laser Applicator into the tissue.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1781-2021·2021-06-09
Tranberg MR Stylet Recalled Due to Inadequate Sterilization
CLINICAL LASERTHERMIA SYSTEMS AB is recalling Tranberg MR Stylet devices (lot IDs 116540030718 and 116540201117) because single-use units labeled as sterile may not have been adequately sterilized, creating infection risk.
Product
Tranberg MR Stylet, 1.8mm/15G, 230mm, REF: 4013-06, Rx Only, Sterile EO - Product Usage: used with the Tranberg¿ MR Introducer; a device used to aid the insertion of the Laser Applicator into the tissue.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1729-2021·2021-06-09
Orthopedic Drill Kit Recalled for Potential Sterilization Failure
Zavation is recalling the ZVplasty Direct Bipedicular Bone Access Kit due to products potentially lacking adequate sterilization. The 15 units affected (Lot 20071774, 19123262) were distributed nationwide.
Product
ZVplasty Direct Bipedicular Bone Access Kit with Drill, 11 Gauge, REF VCF-DDBAK-11. For use in Orthopedic / spinal procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1697-2021·2021-06-09
K2M Cascadia lumbar implants recalled for mislabeled dimensions
K2M, Inc. is recalling Cascadia AN Interbody Convex lumbar implants due to incorrect dimensions listed on product labels for specific lot numbers and device sizes.
Product
Cascadia AN Interbody Convex 10x28x14mm Catalog Number: 6101-2102814NC-G2 Lumbar implants are intervertebral body fusion devices indicated for use with autograft and/or allogenic bone graft comprised of cancellous and/or corticocancellous bone graft when used as anadjunct…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1701-2021·2021-06-09
Cement Delivery Cannula May Not Be Adequately Sterilized
Zavation is recalling 10 gauge cement delivery cannulas (INTVM-CDC) used in orthopedic procedures because distributed products may not have been adequately sterilized. The recall affects 130 units distributed nationwide.
Product
10 GAUGE CEMENT DELIVERY CANNULA, INTVM-CDC. For use in Orthopedic / spinal procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1734-2021·2021-06-09
Zavation 10G Direct Single Bone Access Kit Recall Due to Inadequate Sterilization
Zavation is recalling its 10G Direct Single Bone Access Kit because some units distributed as sterile may not have been adequately sterilized. The kit is used in orthopedic and spinal procedures and was distributed nationwide.
Product
10G DIRECT SINGLE BONE ACCESS KIT. For use in Orthopedic / spinal procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1742-2021·2021-06-09
Orthopedic bone access kits recalled for inadequate sterilization
Zavation recalled its 10G Direct Double Bone Access Kit because some units distributed as sterile may not have been adequately sterilized. Affected devices are used in orthopedic and spinal procedures.
Product
10G DIRECT DOUBLE BONE ACCESS KIT. For use in Orthopedic / spinal procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1759-2021·2021-06-09
ZVplasty Orthopedic Spinal System Units Recalled Due to Inadequate Sterilization
Zavation is recalling 516 units of ZVplasty System (15mm) spinal surgical devices because products distributed as sterile may not have been adequately sterilized. Patients who received this device may face infection risk.
Product
ZVplasty System, 15mm, Part# VCF-1015-1. For use in Orthopedic / spinal procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1764-2021·2021-06-09
Zavation Spinal Balloon Kit Recall Due to Inadequate Sterilization
Zavation is recalling 79 units of the ZVplasty 10G, 15mm Single Balloon Kit due to inadequate sterilization. Affected devices may pose a contamination risk for patients undergoing spinal procedures.
Product
ZVplasty 10G, 15mm Single Balloon Kit, REF VCF-SBK. For use in Orthopedic / spinal procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1731-2021·2021-06-09
10 Gauge Drill for Orthopedic Surgery Recalled for Sterilization Failure
Zavation recalled 58 units of 10 Gauge Drill (Lot 20102486) used in orthopedic/spinal procedures due to potential inadequate sterilization. Patients should contact their surgeon if they received treatment with an affected device.
Product
10 Gauge Drill, CODE: INTVM-DRL. For use in Orthopedic / spinal procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1766-2021·2021-06-09
ZVplasty orthopedic surgical devices may lack adequate sterilization
Zavation is recalling 24 units of the ZVplasty System used in orthopedic and spinal procedures due to potential inadequate sterilization. Patients who received recalled devices should contact their healthcare provider.
Product
ZVplasty System, 20mm, Part# VCF-1020-2. For use in Orthopedic / spinal procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1698-2021·2021-06-09
T25 Cannulated Screwdrivers May Break During Surgical Procedures
T25 Cannulated Screwdrivers (CSD 025) packaged in Guide Wire Kits may break at the driver tip during use, extending surgery time and requiring additional imaging to identify fragments.
Product
T25 Cannulated Screwdrivers (CSD 025) packaged in Guide Wire Kits (GWK 300) - Product Usage: Intended to be used to insert screws with T25 driving features, which includes screws with diameters of 5.5mm, 6.5mm, and 7.3mm Product Code: GWK 300
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1733-2021·2021-06-09
Zavation 10G Beveled Trocar/Cannula Recalled Due to Inadequate Sterilization
Zavation is recalling 10G beveled trocar/cannula instruments used in orthopedic and spinal procedures due to potential inadequate sterilization, creating infection risk.
Product
10G BEVELED TROCAR/CANNULA. For use in Orthopedic / spinal procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·21149·2021-06-09
CamelBak Water Bottle Caps Recalled for Choking Hazard
CamelBak is recalling certain caps sold with Podium and Peak Fitness water bottles because a small silicone valve can come loose and detach, posing a choking hazard. No injuries have been reported.
Product
CamelBak Podium and Peak Fitness water bottles
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1705-2021·2021-06-09
ZVplasty Cement Delivery Cannulas Recalled for Inadequate Sterilization
Zavation recalled 14 units of ZVplasty Bipedicular Cement Delivery Cannula Kits distributed nationwide because they may not have been adequately sterilized.
Product
ZVplasty, Bipedicular Cement Delivery Cannula Kit, 10 Gauge, REF VCF-DCDK. For use in Orthopedic / spinal procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0642-2021·2021-06-09
Clio Yogurt Bars recalled for possible metal fragments
Clio LLC is recalling Clio Yogurt Bar Raspberry/Peach Mini Club pack (24g x 24) due to possible metal fragments in the product.
Product
Clio Yogurt Bar Raspberry / Peach Mini Club pack Clio 24g x 24 (12pc tray). UPC Code:854021008251
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1769-2021·2021-06-09
Zavation Vertebrex Spinal Balloon Kit May Not Be Properly Sterilized
Zavation has recalled 140 units of its Vertebrex Single Balloon Kit used in spinal procedures due to inadequate sterilization. Products marketed as sterile may not meet sterility standards.
Product
VERTEBREX SINGLE BALLOON KIT, REF VBRX-15-SBK-10. For use in Orthopedic / spinal procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1691-2021·2021-06-09
Draeger Evita V800 Ventilator Recalled for Multiple Software Defects
Draeger Medical is recalling the Evita V800 critical care ventilator due to three unrelated software defects affecting ventilation delivery and alarm functionality.
Product
Critical Care Ventilator, Catalog Number(s): 8422500: Evita V800 - Product Usage: used for treating patients who require temporary or longer term respiratory support for different medical reasons.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1758-2021·2021-06-09
Zavation ZVplasty Double Balloon Kit Recalled Due to Inadequate Sterilization
Zavation recalls ZVplasty 10G, 10mm Double Balloon Kits used in spinal surgery due to potential inadequate sterilization. Seven units distributed nationwide may not have met sterility standards.
Product
ZVplasty, 10G, 10mm Double Balloon Kit, REF VCF-1010-DBK. For use in Orthopedic / spinal procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1722-2021·2021-06-09
ZVplasty Biopsy Device Lot 20061369 Recalled for Inadequate Sterilization
Zavation is recalling 162 units of the ZVplasty Biopsy Device (Lot 20061369) used in orthopedic and spinal procedures because they may not have been adequately sterilized.
Product
ZVplasty Biopsy Device, 10 Gauge, REF VCF-1010. For use in Orthopedic / spinal procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1726-2021·2021-06-09
ZVplasty Directional Cement Cannula recalled for inadequate sterilization
Zavation is recalling 11 units of ZVplasty Directional Cement Cannula from lot 20061366 because products distributed as sterile may not have been adequately sterilized. The affected devices were distributed nationwide.
Product
ZVplasty Directional Cement Cannula (4 pieces per pack), REF VCF-1080-S4. For use in Orthopedic / spinal procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1752-2021·2021-06-09
InterV Kyphoplasty Spinal Devices Recalled for Inadequate Sterilization
Zavation's InterV 10G FLEX Kyphoplasty spinal devices are recalled because they may not have been adequately sterilized. The recall affects 178 units distributed nationwide.
Product
InterV, 10G FLEX Kyphoplasty, REF Number: a) INTVM-15-FLDSK b) INTVM-20-FLDSK. For use in Orthopedic / spinal procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1738-2021·2021-06-09
Zavation 10G Direct Double Bone Access Kit May Not Be Properly Sterilized
Zavation recalled its 10G Direct Double Bone Access Kit used in orthopedic surgery because products distributed as sterile may not have been adequately sterilized, potentially exposing patients to infection.
Product
10G DIRECT DOUBLE BONE ACCESS KIT. For use in Orthopedic / spinal procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1739-2021·2021-06-09
11G Direct Double Bone Access Kit May Not Be Adequately Sterilized
Zavation's 11G Direct Double Bone Access Kit for spinal and orthopedic procedures may not have been adequately sterilized during manufacturing. Distributed nationwide, the non-sterile devices may pose infection risks to patients.
Product
11G DIRECT DOUBLE BONE ACCESS KIT. For use in Orthopedic / spinal procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0643-2021·2021-06-09
Clio Yogurt Bars Recalled for Possible Metal Fragments
Clio LLC is recalling Clio Yogurt Bar Mixed Berry Low Sugar Bar 50g x 10 retail 10-packs nationwide due to possible metal fragments in the product.
Product
Clio Yogurt Bar Mixed Berry Low Sugar Bar 50g x 10 Clio Retail 10-pack. UPC Code:854021008190
Category
Food
Distribution
Distributed nationwide