State

Northern Mariana Islands product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

38851–38875 of 73764

HighFDA (Devices)·Z-1357-2018·2018-04-18
Bard Premature Infant Feeding Tubes Recalled for Ineffective Fusion
C.R. Bard is recalling specific lots of Bard Premature Infant Feeding Tubes because the tubing and ENFit connector may not be effectively fused.
Product
Bard(R) Premature Infant Feeding tube, ENFit(TM), REF EN0036430 Product Usage: BARD(R) Nasogastric Sump Tubes with ENFit(TM) connector are intended to be used for: Decompression of stomach by suction or aspiration of gastric contents Short-term administration of term…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1366-2018·2018-04-18
Beckman Coulter iQ200 Urine Analyzer Recall for Barcode Reading Failures
Beckman Coulter is recalling iQ200 Series Urine Microscopy Analyzers because they may fail to read dilution barcodes, causing erroneous results that could delay treatment.
Product
iQ200 Series Urine Microscopy Analyzer with Barcode Reader Model NFT-2100, Catalog #s: 800-3046, 800-3047, 800-3052, 800-3053, 800-3802, 800-3803, 800-3900, 800-3920, 800-3925, 800-3931, 800-3933, 800-3934, 800-3935, 800-3937, 800-3950, 800-3951, 800-3042, 800-3043, 800-3044…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1354-2018·2018-04-18
Bard Premature Infant Feeding Tube Recalled for Ineffective Fusion
C.R. Bard is recalling 42,200 units of Bard Premature Infant Feeding Tubes due to potentially ineffective fusion between the tubing and the ENFit connector.
Product
Bard(R) Premature Infant Feeding Tube, ENFit(TM), REF EN0036400 Product Usage: BARD(R) Nasogastric Sump Tubes with ENFit(TM) connector are intended to be used for: Decompression of stomach by suction or aspiration of gastric contents Short-term administration of term…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0622-2018·2018-04-18
Elroselabs Recalls Molleave OTC Product Due to cGMP Deviations
Elroselabs Inc. is voluntarily recalling Molleave, 2 oz bottles, due to current Good Manufacturing Practice (cGMP) deviations. The product was distributed nationwide.
Product
Molleave, 2 oz bottle, OTC, Manufactured for Elrose Labs, Inc.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1347-2018·2018-04-18
ICU Medical Recalls Infusion Sets with Incorrect Spin Collars
ICU Medical is recalling 7,600 sterile intravascular administration sets because they were manufactured with an incorrect spin collar. The sets were distributed in the US, Canada, and Japan.
Product
14 cm (5.5") Appx 0.27 ml, Smallbore Ext Set w/SURPLUG¿ Nano T-Connector, Clamp, Rotating Luer, 50 pouches per case, Item IR-NG31481B, Sterile, Rx. The firm name on the label is icumedical, San Clemente, CA. The Intravascular Administration Set is a single use, sterile…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0623-2018·2018-04-18
Elroselabs Recalls Conzerol Hydrogen Peroxide Gel Due to cGMP Deviations
Elroselabs Inc. is voluntarily recalling Conzerol Hydrogen Peroxide Gel 3% nationwide due to current Good Manufacturing Practice (cGMP) deviations.
Product
Conzerol (antipoxin) H2O2 Gel, Hydrogen Peroxide Gel 3%, 1.5 oz. tube, OTC, Manufactured for Elrose Labs, Inc., Sanford, FL
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0621-2018·2018-04-18
Elroselabs Recalls Conzerol Topical Cream Due to Manufacturing Deviations
Elroselabs Inc. is voluntarily recalling Conzerol topical cream nationwide due to cGMP deviations. The recall was initiated in March 2018 and terminated in December 2020.
Product
Conzerol zero molluscum contagiosum, Topical Cream, Net weight 0.78 (22g), Elrose Labs, Sanford Fl 32771 USA --- NDC 70223-001-06
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1343-2018·2018-04-18
ICU Medical Recalls Infusion Sets with Incorrect Spin Collars
ICU Medical is recalling specific lots of sterile intravascular administration sets because they were manufactured with an incorrect spin collar.
Product
6.5" (17 cm) Appx. 0.57 ml, Trifuse Ext Set w/3 MicroClave¿ Clear, NanoClave¿ T-Connector, 4 Clamps, Rotating Luer, Item A1254, 50 pouches per case, Sterile, Rx. The firm name on the label is icumedical, San Clemente, CA. The Intravascular Administration Set is a single…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1353-2018·2018-04-18
Certified Safety Mfg Recalls First Aid Kits with Leaking Honeywell Eyewash
Certified Safety Mfg Inc is recalling 748 first aid and emergency kits containing Honeywell eyewash due to leaking bottles. The affected units were distributed nationwide.
Product
First aid/emergency kits containing Honeywell eyewash: CSM kit number Kit/cabinet Description CSM Eyewash# Size: Honeywell Part# K206125 LXXV - 75V " Economy Cabinet 3 Shelf R508016 Eye Wash " 4 oz. 32-000452-0000 K 206154 LXXV - 75V " Deluxe Cabinet ¿3 Shelf RS08016 Eye…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1370-2018·2018-04-18
Teleflex Baker Jejunostomy Tubes Recalled for Missing Latex Warning
Teleflex Medical Europe Ltd is recalling 200 Baker Jejunostomy Tubes because the packaging lacks a required warning that the product contains natural rubber latex.
Product
Baker Jejunostomy Tubes: Product Code Equivalent Code (a) 655300160 655316 (b) 655500200 655520
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1339-2018·2018-04-18
Ethicon Recalls PDS Plus Sutures Due to Incorrect Expiry Date Labeling
Ethicon, Inc. is recalling PDS Plus Antibacterial Sutures because three lots were labeled with a five-year expiry date instead of the correct two-year date.
Product
PDS Plus Antibacterial (Polydioxanone) Suture Size 1 PDS PLUS Violet 27 Single Armed OS-4 Needle
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1342-2018·2018-04-18
ICU Medical Recalls Smallbore Extension Sets with Incorrect Spin Collars
ICU Medical is recalling 11,500 smallbore extension sets manufactured with incorrect spin collars. The affected units were distributed in the US, Canada, and Japan.
Product
6.5" (17 cm) Smallbore Ext Set w/Remv MicroClave¿ Clear, NanoClave¿ T-Connector, Clamp, Rotating Luer, Bulk Non-Sterile, 500 per case, Item A1009-NS, Rx. The firm name on the label is icumedical, San Clemente, CA. The Intravascular Administration Set is a single use…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1369-2018·2018-04-18
Teleflex Recalls Simplastic Suprapubic Puncture Instruments for Missing Latex Warning
Teleflex Medical Europe Ltd is recalling Simplastic Suprapubic Puncture Instruments because the packaging lacks a required warning that the products contain natural rubber latex.
Product
Simplastic Suprapubic Puncture Instruments: Product Code Equivalent Code (a) 650704100 551310 (b) 650704120 551312 (c) 650704160 551316 Product Usage: RUSCH Simplastic Suprapubic Puncture Instruments are indicated for emergency suprapubic…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0624-2018·2018-04-18
FDA Recalls Zhong Hua Jiu Menthol Patches for GMP Deviations
United Pacific Co Ltd is recalling Zhong Hua Jiu (menthol 1%) Patches because they were produced with substandard GMP manufacturing processes.
Product
Zhong Hua Jiu (menthol 1%) Patch, Distributed by United Pacific Company, UPC 6 924938 100226, NDC 53614-001-02
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1345-2018·2018-04-18
ICU Medical Recalls 7-inch Smallbore Infusion Sets with Incorrect Spin Collar
ICU Medical is recalling 2,950 sterile 7-inch smallbore infusion sets because they were manufactured with an incorrect spin collar. The affected lots were distributed in the US, Canada, and Japan.
Product
7" Smallbore Ext Set w/MicroClave¿, Clave¿ T-Connector, Clamp, Rotating Luer, 50 pouches per case, Item B9900-629, Sterile, Rx. The firm name on the label is icumedical, San Clemente, CA. The Intravascular Administration Set is a single use, sterile, non-pyrogenic device…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1340-2018·2018-04-18
Ethicon Recalls PDS Plus Antibacterial Sutures Due to Incorrect Expiry Dates
Ethicon is recalling PDS Plus Antibacterial Sutures because three lots were labeled with an incorrect five-year expiry date instead of the correct two-year date.
Product
PDS Plus Antibacterial (Polydioxanone) Suture Size 0 PDS Plus Violet 36 Single Armed CTB-1 Needle
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0698-2018·2018-04-18
InvaGen Recalls Decitabine for Injection Due to Impurity Failures
InvaGen Pharmaceuticals is recalling Decitabine for Injection because the product failed water content and impurity specifications.
Product
Decitabine for Injection, 50mg per vial, Rx only, Manufactured by: Cipla Ltd., Verna Goa, India, Manufactured for: Cipla USA, Inc., 1560 Sawgrass Corporate Parkway, Suite 130, Sunrise, FL 33323, NDC 69097-285-37
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1338-2018·2018-04-18
Ethicon Recalls PDS Plus Antibacterial Sutures Due to Incorrect Expiry Dates
Ethicon, Inc. is recalling specific lots of PDS Plus Antibacterial Sutures because they were labeled with an incorrect expiry date of five years instead of two.
Product
PDS Plus Antibacterial (Polydioxanone) Suture Size 0 PDS Plus Violet 36 Single Armed CT-1 Needle
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1346-2018·2018-04-18
ICU Medical Recalls Smallbore Extension Sets Due to Incorrect Spin Collar
ICU Medical is recalling 100 pouches of 5-inch Smallbore Extension Sets because they were manufactured with an incorrect spin collar.
Product
5" (13 cm) Smallbore Ext Set w/MicroClave¿, Clave¿ T-Connector, Clamp, Rotating Luer, 50 pouches per case, Item B99066, Sterile, Rx. The firm name on the label is icumedical, San Clemente, CA. The Intravascular Administration Set is a single use, sterile, non-pyrogenic…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1368-2018·2018-04-18
Teleflex Medical Recalls Rectal Catheters Due to Missing Latex Warning
Teleflex Medical Europe Ltd is recalling 6,340 rectal catheters because the packaging lacks a required warning that the product contains natural rubber latex.
Product
Rectal Catheters; Product Code Equivalent Code 580114 580114 Product Usage: Rectal Balloon Catheter is inserted into the rectum to measure the abdominal pressure as bladder filled.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1109-2018·2018-04-18
Diet Pepsi 6-Packs Recalled for Incorrect Aspartame-Free Labeling
Pepsi Cola Bottling Company is recalling Diet Pepsi 6-packs because the outer packaging incorrectly states the product is 'Now Aspartame Free' when it actually contains aspartame.
Product
Diet Pepsi; NOW ASPARTAME FREE; 6 PACK; 16 OZ BOTTLES; 6-16 FLOZ BOTTLES (96 FL OZ)
Category
Food
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1358-2018·2018-04-18
Aesculap Recalls Doyen-Collin Mouth Gags Due to Sticking Plastic Sleeves
Aesculap Implant Systems LLC is recalling Doyen-Collin Mouth Gags because plastic sleeves may stick together, rendering the instruments unusable.
Product
Doyen-Collin Mouth Gag 120MM/ General Instruments
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Food)·F-1013-2018·2018-04-18
Bestco Signature Care Calcium Chews Recalled for Vitamin D Labeling Error
Bestco, Inc. is recalling Signature Care Calcium Chews because the packaging declares 25 mcg of Vitamin D, but the product actually contains 12.5 mcg.
Product
Signature Care Calcium Chews; Dietary Supplement; 500 mg Calcium; 25 mcg Vitamin D; Chocolate; 100 chews; Serving Size 1 chew;
Category
Food
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1352-2018·2018-04-18
Magstim Rapid Therapy System Recalled for Missing User Manuals
The Magstim Company Limited is recalling 43 Magstim Rapid Therapy Systems because user manuals were not supplied with the devices.
Product
Magstim Rapid Therapy System consisting of: Rapid Mainframe, Rapid Single Power Supply Unit , Rapid User Interface, Air Film Coil and Main Filters Product Usage For the treatment of major depressive disorders in adult patients who have failed to achieve satisfactory…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1359-2018·2018-04-18
Aesculap Strauss Penis Clamp Recalled Due to Sticking Plastic Sleeves
Aesculap Implant Systems LLC is recalling Strauss Penis Clamps because plastic sleeves may stick together, rendering the instruments unusable.
Product
Strauss Penis Clamp 130MM/General Instruments
Category
Medical Device
Distribution
Distributed nationwide