State

Northern Mariana Islands product recalls

73,576 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 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27251–27275 of 73599

ModerateFDA (Devices)·Z-0282-2021·2020-10-28
Fujifilm Synapse PACS Software Version 5.6.1 Recalled for CT Measurement Error
Fujifilm is recalling Synapse PACS Software Version 5.6.1 because certain CT studies may report inaccurate 3D Sphere MAX values.
Product
Synapse PACS Software Version 5.6.1 - Product Usage: intended for use as a web based application on an off-the shelf PC which meets or exceeds minimum specifications and is networked with a FUJIFILM Synapse PACS server.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0041-2021·2020-10-28
Killz Germz Hand Sanitizer Recalled for Sub-Potent Ethanol Levels
Genesis Partnership Company SA is recalling Killz Germz Hand Sanitizer because testing showed ethanol levels as low as 62%, below the labeled 70% claim.
Product
Killz Germz Hand Sanitizer, Alcohol Gel, 1 Gallon (128 fl. oz.) bottle, Manufactured by Genesis Partnership Company S.A., Guatemala, For: Killz Germz, LLC., 1912 R street NW, Washington DC 20009, NDC 74625-003-05, UPC 7401037203427.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0166-2021·2020-10-28
Smith & Nephew Recalls OSTEORAPTOR Absorbable Suture Anchors Due to Seal Issues
Smith & Nephew is recalling OSTEORAPTOR absorbable suture anchors because improper or incomplete packaging seals may breach the sterile barrier.
Product
OSTEORAPTOR CRVD 2.3 SA UB COBRD BLACK- Absorbable Suture anchor Product Number: 72203291
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0165-2021·2020-10-28
Smith & Nephew Recalls OSTEORAPTOR Absorbable Suture Anchors Due to Seal Issues
Smith & Nephew is recalling OSTEORAPTOR absorbable suture anchors because improper or incomplete packaging seals may breach the sterile barrier.
Product
OSTEORAPTOR CRVD 2.3 SA UB COBRD BLUE- Absorbable Suture anchor Product Number: 72203290
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0152-2021·2020-10-28
Smith & Nephew Recalls OSTEORAPTOR Suture Anchors Due to Seal Issues
Smith & Nephew is recalling OSTEORAPTOR absorbable suture anchors because improper or incomplete packaging seals may breach the sterile barrier.
Product
OSTEORAPTOR 2.9 W/ 2 UB WHITE / BLUE -Absorbable Suture anchor Product Number: 72201995
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0160-2021·2020-10-28
Smith & Nephew Recalls TWINFIX ULTRA Absorbable Suture Anchors
Smith & Nephew is recalling TWINFIX ULTRA absorbable suture anchors due to improper or incomplete packaging seals that may breach the sterile barrier.
Product
TWINFIX ULTRA PLLA HA 5.5MM W/ NEEDLES- Absorbable Suture anchor Product Number: 72202616
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0151-2021·2020-10-28
Smith & Nephew Recalls OSTEORAPTOR Absorbable Suture Anchors Due to Seal Issues
Smith & Nephew is recalling OSTEORAPTOR absorbable suture anchors because improper or incomplete packaging seals may breach the sterile barrier.
Product
OSTEORAPTOR 2.9 W/ 1 UB COBRAID BLUE -Absorbable Suture anchor Product Number: 72201994
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0150-2021·2020-10-28
Smith & Nephew Recalls OSTEORAPTOR Absorbable Suture Anchors Due to Seal Defects
Smith & Nephew is recalling OSTEORAPTOR absorbable suture anchors because improper or incomplete packaging seals may breach the sterile barrier.
Product
OSTEORAPTOR 2.3 W. UB COBRAID BLUE-Absorbable Suture anchor Product Number: 72201993
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0148-2021·2020-10-28
Smith & Nephew Recalls OSTEORAPTOR Absorbable Suture Anchors Due to Seal Issues
Smith & Nephew is recalling OSTEORAPTOR 2.3 W 1UB II BLUE absorbable suture anchors because improper or incomplete packaging seals may breach the sterile barrier.
Product
OSTEORAPTOR 2.3 W 1UB II BLUE-Absorbable Suture anchor Product Number: 72201991
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0154-2021·2020-10-28
Smith & Nephew Recalls OSTEORAPTOR Absorbable Suture Anchors Due to Seal Defects
Smith & Nephew is recalling OSTEORAPTOR absorbable suture anchors because improper or incomplete packaging seals may breach the sterile barrier.
Product
OSTEORAPTOR 2.9 W 1UB II BLUE--Absorbable Suture anchor Product Number: 72202165
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0040-2021·2020-10-28
Killz Germz Hand Sanitizer Recalled for Sub-Potent Alcohol Levels
Genesis Partnership Company SA is recalling Killz Germz Hand Sanitizer because testing showed ethanol levels as low as 62%, below the labeled 70% claim.
Product
Killz Germz Hand Sanitizer, Alcohol Gel, 450 mL (15 fl oz.) bottle, Manufactured by Genesis Partnership Company S.A., Guatemala, For: Killz Germz, LLC., 1912 R street NW, Washington DC, 20009, NDC 74625-003-04, UPC 7401037203250.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0048-2021·2020-10-28
ANI Pharmaceuticals Recalls Amphetamine Capsules Due to Incorrect Expiration Date
ANI Pharmaceuticals is recalling 34,968 bottles of amphetamine extended-release capsules because they were labeled with a 24-month expiration date instead of 18 months.
Product
DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE — DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE (DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0049-2021·2020-10-28
Mylan Recalls Candesartan Cilexetil and Hydrochlorothiazide Tablets Due to Impurity
Mylan Pharmaceuticals is recalling specific lots of Candesartan Cilexetil and Hydrochlorothiazide tablets due to out-of-specification organic impurities found during routine stability testing.
Product
CANDESARTAN CILEXETIL AND HYDROCHLOROTHIAZIDE — CANDESARTAN CILEXETIL AND HYDROCHLOROTHIAZIDE (CANDESARTAN CILEXETIL AND HYDROCHLOROTHIAZIDE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0045-2021·2020-10-28
ANI Pharmaceuticals Recalls Amphetamine Capsules Due to Incorrect Expiration Date
ANI Pharmaceuticals is recalling 13,248 bottles of amphetamine extended-release capsules because they were labeled with a 24-month expiration date instead of 18 months.
Product
DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE — DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE (DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0044-2021·2020-10-28
ANI Pharmaceuticals Recalls Amphetamine Capsules Due to Incorrect Expiration Date
ANI Pharmaceuticals is recalling specific lots of amphetamine extended-release capsules because they were labeled with a 24-month expiration date instead of 18 months.
Product
DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE — DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE (DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0126-2021·2020-10-28
Invivo MR Coils Recalled for Incorrect IPX1 Water Ingress Rating Label
Invivo Corporation is recalling 12,764 MR Coils because the labels were mistakenly printed with an IPX1 rating symbol, which indicates water ingress protection.
Product
MR Coils The MR Coil is intended to be used in conjunction with a Magnetic Resonance Scanner to produce diagnostic images of the anatomy of interest that can be interpreted by a trained physician.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0043-2021·2020-10-28
ANI Pharmaceuticals Recalls Amphetamine Capsules Due to Incorrect Expiration Date
ANI Pharmaceuticals is recalling 408 bottles of amphetamine extended-release capsules because they were labeled with a 24-month expiration date instead of 18 months.
Product
DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE — DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE (DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0046-2021·2020-10-28
ANI Pharmaceuticals Recalls Amphetamine Capsules Due to Incorrect Expiration Date
ANI Pharmaceuticals is recalling specific lots of amphetamine extended-release capsules because they were labeled with a 24-month expiration date instead of the correct 18-month date.
Product
DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE — DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE (DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0047-2021·2020-10-28
ANI Pharmaceuticals Recalls Amphetamine Capsules Due to Incorrect Expiration Date
ANI Pharmaceuticals is recalling specific lots of amphetamine extended-release capsules because they were labeled with a 24-month expiration date instead of the correct 18-month date.
Product
DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE — DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE (DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·20V657000·2020-10-27
2021 Jeep Cherokee Front Lower Control Arm Fracture Recall
Chrysler is recalling certain 2021 Jeep Cherokee vehicles because the front lower control arms may fracture while driving. This can cause loss of steering control and increase the risk of a crash.
Product
JEEP — JEEP CHEROKEE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V660000·2020-10-27
Suspension snap-ring failure could cause wheel separation on Western Star 4700
Daimler Trucks is recalling certain 2021 Western Star and Freightliner commercial trucks because the steer axle spindle nut snap-ring may be missing or improperly installed, potentially causing wheel separation and increased crash risk.
Product
FREIGHTLINER — FREIGHTLINER, WESTERN STAR CASCADIA, 4900, 5700, 108SD
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V661000·2020-10-27
Braun Recalls 2017-2020 Demers Ambulances for Seat Belt Defect
Braun Ambulances is recalling 2017-2020 Demers TSE and EXE ambulances because the rear seat belt harness may separate from its mounting, increasing injury risk in a crash.
Product
DEMERS AMBULANCES — DEMERS AMBULANCES, DEMERS EXE, TSE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20E082000·2020-10-27
Leather on Wheels Recalls Polo Helmets for Impact Protection Defect
Leather on Wheels is recalling Polo model helmets because they may not adequately reduce impact force, increasing the risk of injury in a crash.
Product
EQUIPMENT:MOTORCYCLE:HELMETS recall
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·20V659000·2020-10-27
Winnebago Era Recalled for Defective Front Seat Belt Anchor Weld Nut
Winnebago is recalling 2012-2021 Era 170X vehicles because a weld nut was installed on the wrong side of the seat belt bracket, reducing retention strength.
Product
WINNEBAGO — WINNEBAGO ERA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V658000·2020-10-27
Audi Recalls 2018-2020 Q7 Vehicles for C-Pillar Padding Defect
Audi is recalling 2018-2020 Q7 vehicles because the C-pillar padding may not absorb enough impact in a crash, increasing injury risk for unbelted occupants.
Product
AUDI — AUDI Q7
Category
Vehicle
Distribution
Distributed nationwide