State

New Hampshire product recalls

73,738 recalls have nationwide distribution and so reach New Hampshire. 4,482 additional recalls listed New Hampshire specifically in their distribution scope.

What the numbers show

Total: 4,482
Critical: 603
Severe: 1,048
Most recent: 2026-10-28

Of the 4,482 recalls naming New Hampshire we have scored against our rubric, 603 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,048 (23%) are Severe.

Which agencies issued them

These figures cover only the 4,482 recalls whose distribution notice names New Hampshire specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

32526–32550 of 78220

HighFDA (Devices)·Z-0529-2020·2019-12-04
Zimmer Biomet Recalls Guide Wires Due to Bacterial Endotoxin and Debris
Zimmer Biomet is recalling specific Aim/Art Guide Wires because elevated levels of bacterial endotoxin and residual debris remain on the devices due to a cleaning issue.
Product
GUIDE WIRE 2.2MM X 28IN, Aim/Art Guide wire, Item No. 809222028 - Product Usage: These instruments and delivery systems are used to facilitate implantation of orthopedic medical devices.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0577-2020·2019-12-04
Boston Scientific Recalls Emerge Monorail PTCA Catheters Due to Coating Defect
Boston Scientific is recalling Emerge Monorail PTCA Dilatation Catheters because they may lack a required hydrophilic coating. The recall covers 14,145 devices distributed nationwide and in Canada.
Product
Emerge Monorail PTCA Dilatation Catheter. Sterilized using ethylene oxide. Packaged in the following sizes: 1. REF/Catalog No. H7493919308200 EMERGE MR, OUS 2.00mm X 8mm; 2. REF/Catalog No. H7493918912200, EMERGE MR US 2.00MM X 12MM; 3. REF/Catalog No.…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0518-2020·2019-12-04
Becton Dickinson Recalls Site~Rite 8 Ultrasound Systems Due to Battery Indicator Defect
Becton Dickinson is recalling 2,215 Site~Rite 8 Ultrasound Systems because the battery indicator may falsely show charge, causing abrupt shutdowns without warning.
Product
Site~Rite 8 Ultrasound Systems-intended for diagnostic ultrasound imaging of the human body. Site~Rite 8 Ultrasound System, Catalog No.9770500 Refurbished, Site~Rite¿ 8 System, Catalog No.9770500R Site~Rite 8 Ultrasound System, Catalog No.9770501 Refurbished Site~Rite¿ 8…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0532-2020·2019-12-04
Zimmer Biomet Recalls Total Elbow Replacement Devices Due to Cleaning Issues
Zimmer Biomet is recalling specific total elbow replacement devices because elevated levels of bacterial endotoxin and residual debris remain on them due to a cleaning issue.
Product
LT DISC ULNA - HA/PC; RT DISC ULNA - HA/PC; LT DISC HMRL- HA/PC; RT DISC HMRL- HA/PC; DISC XS ULNA POR; DISC SEG ULNA POR; and Custom devices Item Nos. 114754 114755 114744 114745 114704 114705 114756 114757 114714 114715 114746 114747 114706 114707…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0534-2020·2019-12-04
Nextremity Solutions Recalls Stratum Foot Plating System Screws Due to Incorrect Specifications
Nextremity Solutions is recalling 49 units of Stratum Foot Plating System screws because they may contain the incorrect screw type and length.
Product
Stratum Foot Plating System-NL LP Screw 3.5x50mm ST, sterile. Catalog Number: STRM-NL-3550ST - Product Usage: The Stratum Foot Plating System is a plate and screws construct indicated for fixation of fractures, osteotomies, nonunions, malunions and fusions of small bones and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0513-2020·2019-12-04
Medline Recalls EVENCARE G3 Blood Glucose Test Strips Due to Seal Defects
Medline Industries is recalling EVENCARE G3 Blood Glucose Test Strips because incomplete seals may cause the strips to expire prematurely.
Product
EVENCARE G3 Blood Glucose Test Strips, 1 test strip per foil pouch, 50 foil pouches per box, 12 boxes per case.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0551-2020·2019-12-04
Boston Scientific Recalls Advanix Pancreatic Stents Due to Shelf Life Labeling Error
Boston Scientific is recalling 54 units of Advanix Pancreatic Stents because they were labeled with a 36-month shelf life instead of the approved 18-month duration.
Product
Advanix Pancreatic Stent, Straight Leading Barb, 10F x 6cm UPN: M00536640
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0545-2020·2019-12-04
Abbott Alinity ci Level Sensor Bulk Solution Recalled for Reliability Issues
Abbott is recalling Alinity ci Level Sensor Bulk Solution kits due to potential cracks caused by environmental stress, which may affect reliability.
Product
Accessory kit, Alinity c containing Alinity ci Level Sensor, Bulk Solution
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0560-2020·2019-12-04
Boston Scientific Pancreatic Stent Recalled for Incorrect Shelf Life Labeling
Boston Scientific is recalling 35 units of Advanix Pancreatic Stents because they were labeled with a 36-month shelf life instead of the approved 18-month shelf life.
Product
Boston Scientific Advanix Pancreatic Stent, Straight Leading Barb, 10F x 18cm UPN: M00536730
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0553-2020·2019-12-04
Boston Scientific Recalls Pancreatic Stents Due to Incorrect Shelf Life Labeling
Boston Scientific is recalling 97 Advanix Pancreatic Stents because they were labeled with a 36-month shelf life instead of the approved 18-month duration.
Product
Boston Scientific Advanix Pancreatic Stent, Straight Leading Barb, 10F x 8cm UPN: M00536660
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0550-2020·2019-12-04
Boston Scientific Pancreatic Stent Recall Due to Incorrect Shelf Life Labeling
Boston Scientific is recalling Advanix Pancreatic Stents because they were labeled with a 36-month shelf life instead of the approved 18-month period.
Product
Boston Scientific Advanix Pancreatic Stent, Straight Leading Barb, 10F x 5cm UPN: M00536630
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0512-2020·2019-12-04
Rocket KCH Fetal Bladder Drainage Catheter Recalled for Kinking and Off-Label Use
Rocket Medical Plc is recalling 1,081 KCH Fetal Bladder Drainage Catheters due to reported kinking and off-label use for pleural drainage.
Product
Rocket KCH Fetal Bladder Drainage Catheter Model: R57405
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0559-2020·2019-12-04
Boston Scientific Recalls Pancreatic Stents Due to Incorrect Shelf Life Labeling
Boston Scientific is recalling 179 Advanix Pancreatic Stents because they were labeled with a 36-month shelf life instead of the approved 18-month shelf life.
Product
Boston Scientific Advanix Pancreatic Stent, Straight Leading Barb, 10F x 15cm UPN: M005337206
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0554-2020·2019-12-04
Boston Scientific Pancreatic Stent Recall Due to Incorrect Shelf Life Labeling
Boston Scientific is recalling Advanix Pancreatic Stents because they were labeled with a 36-month shelf life instead of the approved 18-month shelf life.
Product
Boston Scientific Advanix Pancreatic Stent, Straight Leading Barb, 10F x 9cm UPN: M00536670
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0552-2020·2019-12-04
Boston Scientific Pancreatic Stent Recall Due to Incorrect Shelf Life Labeling
Boston Scientific is recalling 940 Advanix Pancreatic Stents because they were labeled with a 36-month shelf life instead of the approved 18-month shelf life.
Product
Boston Scientific Advanix Pancreatic Stent, Straight Leading Barb, 10F x 7cm UPN: M00536650
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0543-2020·2019-12-04
Abbott Alinity ci Level Sensor Recalled for Potential Cracking
Abbott is recalling Alinity ci Level Sensors, Bulk Solution, because environmental stress may cause cracks that affect reliability.
Product
Alinity ci Level Sensor, Bulk Solution
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0579-2020·2019-12-04
Boston Scientific Recalls NC Emerge Monorail PTCA Catheters for Coating Defect
Boston Scientific is recalling NC Emerge Monorail PTCA Dilatation Catheters because they may be missing a hydrophilic coating step during manufacturing.
Product
NC Emerge Monorail PTCA Dilatation Catheter. Sterilized using ethylene oxide. Packaged in the following sizes: 1. REF/Catalog No. H7493926708350, NC EMERGE MR US 3.50MM X 8MM; 2. REF/Catalog No. H7493927608350, NC EMERGE MR OUS 3.50MM X 8MM; 3. REF/Catalog No.…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0548-2020·2019-12-04
Boston Scientific Recalls Pancreatic Stents Due to Incorrect Shelf Life Labeling
Boston Scientific is recalling 109 units of Advanix Pancreatic Stents because they were labeled with a 36-month shelf life instead of the approved 18-month shelf life.
Product
Boston Scientific Advanix Pancreatic Stent, Straight Leading Barb, 10F x 3cm UPN: M00536610
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0549-2020·2019-12-04
Boston Scientific Recalls Pancreatic Stents Due to Incorrect Shelf Life Labeling
Boston Scientific is recalling 66 units of Advanix Pancreatic Stents because they were labeled with a 36-month shelf life instead of the approved 18-month shelf life.
Product
Boston Advanix Pancreatic Stent, Straight Leading Barb, 10F x 4cm UPN: M00536620
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0556-2020·2019-12-04
Boston Scientific Recalls Pancreatic Stents Due to Incorrect Shelf Life Labeling
Boston Scientific is recalling 139 units of Advanix Pancreatic Stents because they were labeled with a 36-month shelf life instead of the approved 18-month shelf life.
Product
Boston Scientific Advanix Pancreatic Stent, Straight Leading Barb, 10F x 11cm UPN: M005336690
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0558-2020·2019-12-04
Boston Scientific Recalls Pancreatic Stents Due to Incorrect Shelf Life Labeling
Boston Scientific is recalling 66 units of Advanix Pancreatic Stents because they were labeled with a 36-month shelf life instead of the approved 18-month shelf life.
Product
Boston Scientific Advanix Pancreatic Stent, Straight Leading Barb, 10F x 13cm UPN: M00536710
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0557-2020·2019-12-04
Boston Scientific Recalls Pancreatic Stents Due to Incorrect Shelf Life Labeling
Boston Scientific is recalling 271 Advanix Pancreatic Stents because they were labeled with a 36-month shelf life instead of the approved 18-month shelf life.
Product
Boston Scientific Advanix Pancreatic Stent, Straight Leading Barb, 10F x 12cm UPN: M00536700
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0544-2020·2019-12-04
Abbott Alinity i Accessory Kit Recalled for Potential Sensor Cracks
Abbott is recalling Alinity i accessory kits because environmental stress may cause cracks in the bulk solution level sensor.
Product
Accessory kit, Alinity i containing Alinity ci Level Sensor, Bulk Solution
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0555-2020·2019-12-04
Boston Scientific Recalls Pancreatic Stents with Incorrect Shelf Life Labeling
Boston Scientific is recalling Advanix Pancreatic Stents labeled with a 36-month shelf life instead of the approved 18-month duration.
Product
Boston Scientific Advanix Pancreatic Stent, Straight Leading Barb, 10F x 10cm UPN: M005336680
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0578-2020·2019-12-04
Boston Scientific Recalls Guidezilla II Catheters Due to Missing Coating
Boston Scientific is recalling Guidezilla II Guide Extension Catheters because they may lack a hydrophilic coating, potentially affecting device performance.
Product
Guidezilla II Guide Extension Catheter Sterilized using ethylene oxide. Packaged in the following sizes: 1. REF/Catalog No. H7493933515060, 6F; 2. REF/Catalog No H7493933515070, 7F.
Category
Medical Device
Distribution
Distributed nationwide