State

American Samoa product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

32151–32175 of 73762

CriticalFDA (Devices)·Z-2460-2019·2019-09-18
Allergan Recalls Textured Breast Implants Due to Lymphoma Risk
Allergan is recalling specific textured breast implants and tissue expanders following FDA safety updates regarding a higher incidence of anaplastic large cell lymphoma (BIA-ALCL).
Product
Natrelle and McGhan 410 TruForm 2 (Soft Touch) BIOCELL breast implant, Styles LL, LM, LF, ML, MM, MF, FL, FM, FF Product Usage: Breast augmentation and Breast reconstruction
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2497-2019·2019-09-18
Aesculap Caiman Disposable Surgical Instrument Recalled for Sterility Concerns
Aesculap Implant Systems LLC is recalling Caiman disposable articulated instruments due to a possibility that the sterility batch was insufficiently sterilized.
Product
CAIMAN DISP.INSTR.ARTICULAT.D:12/440MM REF: PL731SU- Product Usage: Instrument intended for use in general surgery and gynecologic procedures where ligation and division of vessels is desired.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2451-2019·2019-09-18
Allergan Recalls Natrelle Textured Breast Implants Due to Lymphoma Risk
Allergan PLC is recalling Natrelle textured breast implants and tissue expanders worldwide due to an increased risk of anaplastic large cell lymphoma.
Product
Natrelle, Saline-Filled Breast Implant Biocell Full Height with Fill Tube, Sterile, for the following style numbers: Style 163:163-360CC, 163-440CC, 163-530CC, 163-655CC, 163-780CC; Style…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2453-2019·2019-09-18
Allergan Recalls Textured Breast Implants Due to Lymphoma Risk
Allergan is recalling textured Natrelle Inspira breast implants and tissue expanders following FDA safety updates linking these devices to a higher incidence of anaplastic large cell lymphoma.
Product
Natrelle Inspira, Silicone-Filled Breast Implants, Sterile, for the following style numbers: Style TRL: TRL-110TRL-125,TRL-140,TRL-170,TRL-200,TRL-230,TRL-260,TRL-290,TRL-320,TRL-350,TRL-380,TRL-410,TRL-460,TRL-510,TRL-560,TRL-610; Style TRLP…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2311-2019·2019-09-18
Teleflex Recalls Sheridan LTS Tracheal Tubes Due to Disconnection Risk
Teleflex Medical is recalling specific lots of Sheridan LTS tracheal tubes because the 15 mm connector may disconnect from the tube, potentially causing insufficient oxygenation.
Product
Hudson RCI Sheridan LTS: a) 4.0 mm, REF 5-11108 b) 5.0 mm, REF 5-11110 c) 6.0 mm, REF 5-11112 Product Usage: Tracheal tube/airway management
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2456-2019·2019-09-18
Allergan Recalls Natrelle Tissue Expanders Due to Lymphoma Risk
Allergan is recalling Natrelle tissue expanders because the FDA identified a higher incidence of anaplastic large cell lymphoma in patients with textured breast implants.
Product
Natrelle133 Plus Tissue Expander With/Without Suture Tabs, BioCell Full Height Variable Projection with Magna-Fider Xact & 21G Needle Infusion Set, Sterile, for the following style numbers: STYLE 133P-FV: 133P-FV-11, 133P-FV-12, 133P-FV-13, 133P-FV-14, 133P-FV-15…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1852-2019·2019-09-18
Pfizer Recalls Bacteriostatic Water Vials Due to Sterility Concerns
Pfizer is recalling 185,700 vials of Bacteriostatic Water for Injection due to a lack of assurance of sterility. The product was distributed nationwide in the US and Puerto Rico.
Product
BACTERIOSTATIC WATER — BACTERIOSTATIC WATER (BACTERIOSTATIC WATER)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-2123-2019·2019-09-18
Bubbies Ice Cream Products Recalled for Foreign Plastic Pieces
Bubbies is recalling Mochi and Cookie Dough Ice Cream Bites due to potential foreign plastic pieces. The recall covers products distributed nationwide and to Russia and Lebanon.
Product
Bubbies Cookie Dough Ice Cream Bites -Chocolate Chip Item Code CDR00002, UPC Code 50013-1, UPC GTIN 10787325500138. Product is packed in oriented polystyrene sheet (OPS) thermo-formed 6-cavity trays, tray is packed in 6 count boxes.
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2463-2019·2019-09-18
Allergan Recalls Textured Breast Implants Due to Lymphoma Risk
Allergan PLC is recalling specific textured breast implants and tissue expanders following FDA safety updates regarding a higher incidence of anaplastic large cell lymphoma (BIA-ALCL).
Product
Komuro, Soft Touch, BIOCELL, INTRASHIEL, BioDIMENSIONAL breast implants, Styles KML, KMM, KLL, KLM Product Usage: Breast augmentation and Breast reconstruction
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2462-2019·2019-09-18
Allergan Recalls Textured Silicone-Filled Breast Implants Due to Lymphoma Risk
Allergan PLC is recalling specific textured silicone-filled breast implants and tissue expanders following FDA safety updates regarding a higher incidence of anaplastic large cell lymphoma (BIA-ALCL).
Product
Natrelle and McGhan Silicone-Filled Breast Implants, TruForm 2 (Soft Touch), BIOCELL, Styles 110 Soft Touch and 120 Soft Touch Product Usage : Breast augmentation and Breast reconstruction
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·19V661000·2019-09-18
4-Star Horse Trailer Recall for Insufficient Axle Bearing Grease
4-Star Trailers is recalling 2019 horse trailers because axle bearings may lack proper grease, increasing the risk of wheel lockup and crashes.
Product
4-STAR TRAILER — 4-STAR TRAILER HORSE TRAILER
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2317-2019·2019-09-18
Teleflex Recalls Sheridan/CF Novaplus Tracheal Tubes Due to Connector Disconnection
Teleflex Medical is recalling Sheridan/CF Novaplus 7.0 mm tracheal tubes because the Sheridan connector may disconnect from the tube, potentially causing insufficient oxygenation.
Product
Sheridan/CF Novaplus 7.0 mm, REF V5-10114 Product Usage: Tracheal tube/airway management
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·19V663000·2019-09-18
Isuzu NPR, NQR, and NRR Recall for Dual Steering Keystock Defect
Diesel Modification Center is recalling 2018-2019 Isuzu NPR, NQR, and NRR vehicles modified with dual steering because a keystock may dislodge, causing loss of steering.
Product
ISUZU — ISUZU NRR, NQR, NPR
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2464-2019·2019-09-18
Allergan Textured Breast Implants Recalled Due to Lymphoma Risk
Allergan is recalling textured breast implants and tissue expanders following FDA safety updates regarding a higher incidence of anaplastic large cell lymphoma (BIA-ALCL).
Product
RITZ PRINCESS, BIOCELL, INTRASHIEL, BioDIMENSIONAL Breast Implant, Styles RML, RMM, RFL, RFM Product Usage: Breast augmentation and Breast reconstruction
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2455-2019·2019-09-18
Allergan Recalls Natrelle Textured Breast Implants and Tissue Expanders
Allergan PLC is recalling Natrelle 133 tissue expanders due to a higher incidence of anaplastic large cell lymphoma (BIA-ALCL) associated with textured breast implants.
Product
Natrelle 133 Tissue Expanders (also named style 133 BIOSPAN Tissue Expander and Mcghan Magna-Site Tissue Expander) BioCell Full Height Variable Projection with Magna-Fider Xact & 21G Needle Infusion Set, Sterile, for the following style numbers: STYLE 133FV: 133FV-11…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2459-2019·2019-09-18
Allergan Recalls McGhan BioDIMENSIONAL Silicone-Filled Breast Implants
Allergan PLC is recalling McGhan BioDIMENSIONAL silicone-filled breast implants due to a higher incidence of anaplastic large cell lymphoma (BIA-ALCL) associated with textured implants.
Product
McGhan BioDIMENSIONAL silicone-Filled Breast Implants, style 153 Product Usage: Breast augmentation and Breast reconstruction
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2315-2019·2019-09-18
Teleflex Recalls Hudson RCI Sheridan Uncuffed Tracheal Tubes
Teleflex Medical is recalling Hudson RCI Sheridan Uncuffed tracheal tubes because specific lots of the 15 mm connector may disconnect from the tube, potentially causing insufficient oxygenation.
Product
Hudson RCI Sheridan Uncuffed: a) 2.0 mm, REF 5-10404 b) 2.5 mm, REF 5-10405 c) 3.0 mm, REF 5-10406 d) 3.5 mm, REF 5-10407 e) 4.0 mm, REF 5-10408 f) 4.5 mm, REF 5-10409 g) 5.0 mm, REF 5-10410 h) 5.5 mm, REF 5-10411 i) 6.0 mm, REF 5-10412 j) 6.5 mm, REF 5-10413 k) 7.0…
Category
Medical Device
Distribution
Distributed nationwide
SevereCPSC·19206·2019-09-18
Kichler Elan Shayla Mini Pendant Lights Recalled for Fire Hazard
Kichler Lighting is recalling Elan Shayla Mini Pendant Lights because the sockets can overheat and catch fire. Consumers should stop using the fixtures and contact Kichler for a free replacement.
Product
Elan Shayla Mini Pendant Lights
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2465-2019·2019-09-18
Allergan Textured Breast Implants Recalled Due to Lymphoma Risk
Allergan is recalling textured breast implants worldwide due to an increased risk of anaplastic large cell lymphoma (BIA-ALCL). Patients should consult their healthcare providers.
Product
Natrelle 150 Full Height and Short Height Implants, BIOCELL, INTRASHIEL, BioDIMENSIONAL Breast Implant, Styles 150 FH and 150 SH. Product Usage: Breast augmentation and Breast reconstruction
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·19V664000·2019-09-18
Subaru Recalls 2020 Legacy and Outback for Brake Pedal Bolt Issue
Subaru is recalling 2020 Legacy and Outback vehicles because a missing or loose brake pedal bolt may reduce braking performance and increase crash risk.
Product
SUBARU — SUBARU LEGACY, OUTBACK
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2313-2019·2019-09-18
Teleflex Recalls Sheridan EZ-ENDO Tracheal Tubes Due to Disconnection Risk
Teleflex Medical is recalling specific lots of Sheridan EZ-ENDO tracheal tubes because the 15 mm connector may disconnect, potentially causing insufficient oxygenation.
Product
Hudson RCI Sheridan EZ-ENDO: a) 5.0 mm, REF 5-22510 b) 5.5 mm, REF 5-22511 c) 7.0 mm, REF 5-22514 d) 7.5 mm, REF 5-22515 e) 8.0 mm, REF 5-22516 f) 8.5 mm, REF 5-22517 g) 9.0 mm, REF 5-22518 h) 6.0 mm, REF 5-22512 i) 6.5 mm, REF 5-22513 Product Usage: Tracheal…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2461-2019·2019-09-18
Allergan Recalls Textured Breast Implants Due to Lymphoma Risk
Allergan is recalling 4 million textured breast implants and tissue expanders worldwide due to an increased risk of anaplastic large cell lymphoma.
Product
Natrelle 510, TruForm, Dual-Gel, BIOCELL, Styles LX, MX, FX Product Usage: Breast augmentation and Breast reconstruction
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2318-2019·2019-09-18
Teleflex Recalls Sheridan/HVT Novaplus Tracheal Tubes Due to Disconnection Risk
Teleflex Medical is recalling specific lots of Sheridan/HVT Novaplus tracheal tubes because the 15 mm Sheridan connector may disconnect from the tube, potentially causing insufficient oxygenation.
Product
Sheridan/HVT Novaplus: a) 7.0 mm, REF V5-10314 b) 7.5 mm, REF V5-10315 c) 8.0 mm, REF V5-10316 d) 8.5 mm, REF V5-10317 Product Usage: Tracheal tube/airway management
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·19V665000·2019-09-18
Mercedes-Benz and Freightliner Sprinter Recalled for Hood Latch Defect
Daimler Vans USA is recalling 2018-2019 Sprinter vans because an improperly tightened hood screw may allow the hood to open while driving, increasing crash risk.
Product
FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 3500, SPRINTER 4500, SPRINTER 1500, SPRINTER 2500
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2316-2019·2019-09-18
Teleflex Medical Recalls Hudson RCI Sheridan/HVT Tracheal Tubes
Teleflex Medical is recalling specific lots of Hudson RCI Sheridan/HVT tracheal tubes because the 15 mm Sheridan connector may disconnect from the tube, potentially causing insufficient oxygenation.
Product
Hudson RCI Sheridan/HVT: a) 5.0 mm, REF 5-10310 b) 5.5 mm, REF 5-10311 c) 6.0 mm, REF 5-10312 d) 6.5 mm, REF 5-10313 e) 7.0 mm, REF 5-10314 f) 7.5 mm, REF 5-10315 g) 8.0 mm, REF 5-10316 h) 8.5 mm, REF 5-10317 i) 9.0 mm, REF 5-10318 j) 10.0 mm, REF 5-10320 Product…
Category
Medical Device
Distribution
Distributed nationwide