State

American Samoa product recalls

73,806 recalls have nationwide distribution and so reach American Samoa. 25 additional recalls listed American Samoa specifically in their distribution scope.

What the numbers show

Total: 25
Critical: 1
Severe: 9
Most recent: 2026-09-09

Of the 25 recalls naming American Samoa we have scored against our rubric, 1 (4%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 9 (36%) are Severe.

Which agencies issued them

These figures cover only the 25 recalls whose distribution notice names American Samoa specifically. The 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

39951–39975 of 73831

HighFDA (Devices)·Z-0413-2018·2018-02-07
Ormco/Sybronendo Recalls Elements Obturation Units and Buchanan Heat Pluggers
Ormco/Sybronendo is recalling 25,765 Elements Obturation Units and Buchanan Heat Pluggers because the pluggers may overheat during use.
Product
Elements Obturation Unit (EOU) used with respective Buchanan Heat Pluggers Device is an endodontic root canal plugger. It is intended to be used in Dentistry to provide continuous heat at the tip of a dental instrument to test tooth response to thermal stimulus, for tissue…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0465-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing rework process caused set screws and sleeves to shift, potentially preventing proper assembly.
Product
Affixus Hip Fracture Nail, RH 130 DEG 11MM X 320MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0436-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing defect may prevent proper assembly of the device.
Product
Affixus Hip Fracture Nail, LH 130 DEG 11MM X 400MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0435-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing defect may prevent the device from being properly assembled.
Product
Affixus Hip Fracture Nail, LH 130 DEG 11MM X 380MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0429-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing defect may prevent the set screw and sleeve assembly from staying in place.
Product
Affixus Hip Fracture Nail, LH 125 DEG 9MM X 380MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0479-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a set screw and sleeve assembly may have shifted, preventing proper product assembly.
Product
Affixus Hip Fracture Nail, RH 130 DEG 9MM X 340MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0441-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing rework process may have displaced internal components, potentially preventing proper assembly.
Product
Affixus Hip Fracture Nail, LH 130 DEG 9MM X 280MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0463-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing rework error may have displaced internal components, potentially preventing proper assembly.
Product
Affixus Hip Fracture Nail, RH 130 DEG 11MM X 280MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0500-2018·2018-02-07
Beaver-Visitec Recalls Safety Knives Due to Retracted Protective Shield
Beaver-Visitec International Inc. is recalling specific EdgeAhead Safety Knives because the protective shield retracted, exposing the blade.
Product
bvi Beaver EdgeAhead Safety Knife, (a) Sideport MVR .90mm 20G, REF 370531 (b) Sideport Angled, .60mm (23G), REF 378233 Product Usage: Specialty blades and knives are used for stab and cut incisions in ophthalmic, ENT and other surgical applications.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0476-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a set screw and sleeve assembly may have shifted, preventing proper assembly.
Product
Affixus Hip Fracture Nail, RH 130 DEG 9MM X 260MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0478-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing rework error may have displaced internal components, potentially preventing proper assembly.
Product
Affixus Hip Fracture Nail, RH 130 DEG 9MM X 320MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0494-2018·2018-02-07
Horiba Medical Recalls ABX PENTRA Reagent Cups for Fit Issues
Horiba Medical is recalling 15 mL reagent cups for ABX PENTRA analyzers because they may not sit properly in the rack, potentially causing incorrect test results without an alarm.
Product
15 ML REAGENT CUP, B1037307, SAP 1221037307 for use with ABX PENTRA 400 / PENTRA C400
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0487-2018·2018-02-07
GE Healthcare CARESCAPE Central Station software recall for communication issues
GE Healthcare is recalling CARESCAPE Central Station software version 2.0.2 because units may experience unexpected network communication issues after boot-up or restart.
Product
GE HEALTHCARE CARESCAPE Central Station (CSCS) software version 2.0.2 The CARESCAPE Central Station is intended to collect information from a network and display this data. This data includes physiological, patient demographic and/or other non-medical information.…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0438-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing rework error may have displaced internal components, potentially preventing proper assembly.
Product
Affixus Hip Fracture Nail, LH 130 DEG 11MM X 440MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0433-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing rework error may have displaced internal components, preventing proper assembly.
Product
Affixus Hip Fracture Nail, LH 130 DEG 11MM X 300MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0426-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Assembly Defect
Zimmer Biomet is recalling 638 units of Affixus Hip Fracture Nails because a manufacturing defect may prevent proper assembly of the device.
Product
Affixus Hip Fracture Nail, LH 125 DEG 11MM X 440MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0484-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing defect may prevent proper assembly of the device.
Product
Affixus Hip Fracture Nail, RH 130 DEG 9MM X 440MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0425-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Assembly Defect
Zimmer Biomet is recalling 638 units of the Affixus Hip Fracture Nail because a manufacturing rework error may have displaced internal components, preventing proper assembly.
Product
Affixus Hip Fracture Nail, LH 125 DEG 11MM X 360MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0467-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing defect may prevent proper assembly of the device.
Product
Affixus Hip Fracture Nail, RH 130 DEG 11MM X 360MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0430-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Assembly Defect
Zimmer Biomet is recalling 638 units of the Affixus Hip Fracture Nail because a manufacturing defect may prevent proper assembly of the device.
Product
Affixus Hip Fracture Nail, LH 125 DEG 9MM X 440MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0439-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Assembly Defect
Zimmer Biomet is recalling 638 units of Affixus Hip Fracture Nails because a set screw and sleeve assembly may have shifted during rework, potentially preventing proper product assembly.
Product
Affixus Hip Fracture Nail, LH 130 DEG 11MM X 460MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0480-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Assembly Defect
Zimmer Biomet is recalling Affixus Hip Fracture Nails because a set screw and sleeve assembly may have shifted, preventing proper installation.
Product
Affixus Hip Fracture Nail, RH 130 DEG 9MM X 360MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0427-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing rework process caused set screws and sleeves to shift, potentially preventing proper assembly.
Product
Affixus Hip Fracture Nail, LH 125 DEG 9MM X 260MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0428-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because set screws and sleeves were found out of place during rework, potentially preventing proper assembly.
Product
Affixus Hip Fracture Nail, LH 125 DEG 9MM X 340MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0452-2018·2018-02-07
Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a set screw and sleeve assembly may have shifted during rework, potentially preventing proper product assembly.
Product
Affixus Hip Fracture Nail, RH 125 DEG 13MM X 260MM
Category
Medical Device
Distribution
Distributed nationwide