State

Northern Mariana Islands product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

41851–41875 of 73829

SevereFDA (Drugs)·D-1004-2017·2017-08-02
SCA Pharmaceuticals Recalls Phenylephrine HCl Bags Due to Sterility Concerns
SCA Pharmaceuticals is recalling two bags of Phenylephrine HCl 10 mg in 0.9% Sodium Chloride because they were made with recalled saline bags that may leak.
Product
PHENYLephrine HCl 10 mg in 0.9% Sodium Chloride, (Final Concentration = 0.1 mg per mL), Total Volume 100 mL Single Dose Container bag, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct, Little Rock, AR 72205 (877) 550-5059; NDC: 70004-0810-32.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1031-2017·2017-08-02
SCA Pharmaceuticals Recalls Phenylephrine Injection Due to Sterility Concerns
SCA Pharmaceuticals is recalling specific lots of Phenylephrine 50 mg injection due to a lack of assurance of sterility and potential for product leakage.
Product
PHENYLephrine 50 mg in 0.9% Sodium Chloride 250 mL, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0820-40
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1018-2017·2017-08-02
SCA Pharmaceuticals Recalls Ephedrine Sulfate Syringes Due to Sterility Concerns
SCA Pharmaceuticals is recalling ePHEDrine Sulfate syringes due to a lack of assurance of sterility and potential for leaking.
Product
ePHEDrine Sulfate 5 mg/mL in NS 5 mL Fill in 12 mL Syringe (25 mg), Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0600-11
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1003-2017·2017-08-02
SCA Pharmaceuticals Recalls Magnesium Sulfate Injection Bags Due to Sterility Concerns
SCA Pharmaceuticals is recalling 40 bags of Magnesium Sulfate 4 g in 0.9% Sodium Chloride because they were made with recalled saline bags that may leak, compromising sterility.
Product
MAGNESIUM Sulfate 4 g added to 100 mL 0.9% Sodium Chloride, Total Approximate Volume 108 mL (does not include mfg. overfill) Single Dose Container bag, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct, Little Rock, AR 72205 (877) 550-5059; NDC: 70004-0737-32.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1025-2017·2017-08-02
SCA Pharmaceuticals Recalls Phenylephrine HCl Bags Due to Sterility Concerns
SCA Pharmaceuticals is recalling specific lots of Phenylephrine HCl 10 mg in 0.9% Sodium Chloride 250 mL bags because they may leak and lack assurance of sterility.
Product
PHENYLephrine HCl 10 mg in 0.9% Sodium Chloride 250 mL Bag, Preservative Free, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0811-40
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1020-2017·2017-08-02
SCA Pharmaceuticals Recalls NORepinephrine Injection Due to Sterility Concerns
SCA Pharmaceuticals is recalling NORepinephrine 4 mg in 0.9% Sodium Chloride 250 mL due to lack of assurance of sterility and potential for leaking.
Product
NORepinephrine 4 mg in 0.9% Sodium Chloride 250 mL from Stock, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0771-40
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1026-2017·2017-08-02
SCA Pharmaceuticals Recalls Phenylephrine IV Bags Due to Sterility Concerns
SCA Pharmaceuticals is recalling specific lots of Phenylephrine 10 mg IV bags due to a lack of assurance of sterility and potential for leaking.
Product
PHENYLephrine 10 mg in 0.9% Sodium Chloride 250 mL bag, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 ---- NDC# 70004-0811-59
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1002-2017·2017-08-02
SCA Pharmaceuticals Recalls Diltiazem Injection Bags Due to Sterility Concerns
SCA Pharmaceuticals is recalling Diltiazem 125 mg injection bags because they were made with recalled saline bags that may leak, compromising sterility.
Product
Diltiazem 125 mg in 0.9% Sodium Chloride, 1 mg per mL, Total Volume 125 mL Single Dose Container bag, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct, Little Rock, AR 72205 (877) 550-5059; NDC: 70004-0541-35.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1022-2017·2017-08-02
SCA Pharmaceuticals Recalls Repinephrine Bitartrate Due to Sterility Concerns
SCA Pharmaceuticals is recalling Repinephrine Bitartrate 16 mg in 0.9% Sodium Chloride 250 mL due to a lack of assurance of sterility and potential for product leakage.
Product
NORepinephrine Bitartrate 16 mg in 0.9% Sodium Chloride 250 mL from Stock, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0775-40
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·17V486000·2017-08-02
CSI Recalls 2013-2016 Wildland Units Due to Wheel Cracking
CSI Emergency Apparatus is recalling 2013-2016 Wildland Emergency vehicles because Stazworks wheels may crack and break, potentially causing a crash.
Product
CSI — CSI WILDLAND UNIT
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1027-2017·2017-08-02
SCA Pharmaceuticals Recalls Phenylephrine Injection Due to Sterility Concerns
SCA Pharmaceuticals is recalling Phenylephrine 40 mg in 0.9% Sodium Chloride 250 mL due to lack of assurance of sterility and potential for leaking.
Product
PHENYLephrine 40 mg in 0.9% Sodium Chloride 250 mL, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0812-40
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1010-2017·2017-08-02
SCA Pharmaceuticals Recalls Fentanyl Syringes Due to Sterility Concerns
SCA Pharmaceuticals is recalling fentanyl citrate syringes due to a lack of assurance of sterility and potential for leaking.
Product
fentaNYL as citrate 5 mcg/mL in 0.9% Sodium Chloride 1 mL in Single Dose syringe, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0225-24
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1006-2017·2017-08-02
SCA Pharmaceuticals Recalls Bupivacaine HCl Bags Due to Sterility Concerns
SCA Pharmaceuticals is recalling specific lots of Bupivacaine HCl 0.125% bags due to a lack of assurance of sterility and potential for leaking.
Product
BUPIVacaine HCl 0.125% In 250 mL 0.9% Sodium Chloride Bag, Preservative Free (Total Dose Bupivacaine 312.5 mg per 250 mL), Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0062-40
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1030-2017·2017-08-02
SCA Pharmaceuticals Recalls Phenylephrine IV Bags Due to Sterility Concerns
SCA Pharmaceuticals is recalling Phenylephrine 20 mg IV bags due to a lack of assurance of sterility and potential for leaking.
Product
PHENYLephrine 20 mg in 0.9% Sodium Chloride 250 mL Bag, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0816-40
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1023-2017·2017-08-02
SCA Pharmaceuticals Recalls Phenylephrine HCl Injection Due to Sterility Concerns
SCA Pharmaceuticals is recalling specific lots of Phenylephrine HCl injection because the product lacks assurance of sterility and has the potential to leak.
Product
PHENYLephrine HCl 60 mg in 0.9% Sodium Chloride 250 mL, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0809-40
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1033-2017·2017-08-02
SCA Pharmaceuticals Recalls Potassium Chloride Injection Due to Sterility Concerns
SCA Pharmaceuticals is recalling specific lots of Potassium Chloride 40 meq Added to Sodium Chloride 0.9% 250 mL due to lack of assurance of sterility and potential for leaking.
Product
Potassium Chloride 40 meq Added to Sodium Chloride 0.9% 250 mL, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 ---- NDC# 70004-0833-40
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1015-2017·2017-08-02
SCA Pharmaceuticals Recalls Fentanyl and Bupivacaine Infusion Bags Due to Sterility Concerns
SCA Pharmaceuticals is recalling specific lots of fentanyl and bupivacaine infusion bags because they may leak and lack assurance of sterility.
Product
fentaNYL 2 mcg/mL + BUPIvacaine 0.125% PF in 0.9% Sodium Chloride 250 mL, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0254-40
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1019-2017·2017-08-02
SCA Pharmaceuticals Recalls Epinephrine HCl Due to Sterility Concerns
SCA Pharmaceuticals is recalling Epinephrine HCl 4 mg in 0.9% Sodium Chloride 250 mL due to a lack of assurance of sterility and potential for leaking.
Product
EPINEPHrine HCl 4 mg in 0.9% Sodium Chloride 250 mL, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0613-40
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1000-2017·2017-08-02
SCA Pharmaceuticals Recalls Fentanyl Citrate Injection Bags Due to Sterility Concerns
SCA Pharmaceuticals is recalling 130 bags of fentanyl citrate injection due to a lack of assurance of sterility caused by potential leaks in the sodium chloride bags used.
Product
fentaNYL (as citrate) 10 mcg per mL in 0.9% Sodium Chloride, (Total fentaNYL Dose 1,000 mcg/100 mL), Total Volume 100 mL Single Dose Container bag, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct, Little Rock, AR 72205 (877) 550-5059; NDC: 70004-0202-32.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1017-2017·2017-08-02
SCA Pharmaceuticals Recalls Hydromorphone Syringes Due to Sterility Concerns
SCA Pharmaceuticals is recalling specific lots of Hydromorphone injection syringes because they may leak and lack assurance of sterility.
Product
Hydromorphone 0.5 mg/mL in 0.9% Sodium Chloride 1 mL Fill in 3 mL BD syringe, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0302-05
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1005-2017·2017-08-02
SCA Pharmaceuticals Recalls Bupivacaine HCl Due to Sterility Concerns
SCA Pharmaceuticals is recalling Bupivacaine HCl 0.1% bags due to a lack of assurance of sterility and potential for leaking.
Product
BUPIVacaine HCl 0.1% PF (From 0.75%) in 0.9% Sodium Chloride, 250 mL Bag, Preservative Free (Waste From 250 mL Bag), Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0060-40
Category
Drug
Distribution
Distributed nationwide
HighCPSC·17197·2017-08-02
Sweet Bamboo Recalls Children's Pajamas for Flammability Violation
Sweet Bamboo is recalling about 500 children's woven pajama sets because they fail to meet federal flammability standards, posing a risk of burn injuries.
Product
Children's two-piece woven pajama sets
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·17V485000·2017-08-02
2017 Jeep Renegade Recall for Instrument Panel Software Defect
Chrysler is recalling 2017 Jeep Renegade vehicles because a software issue may cause malfunction indicator lamps to illuminate incorrectly, potentially masking true vehicle faults.
Product
JEEP — JEEP RENEGADE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2778-2017·2017-08-02
Invuity PhotonBlade Recalled for Potential Unintended Energy Discharge
Invuity, Inc. is recalling 1,328 units of the INVUITY PhotonBlade device due to reports of unintended energy discharge that could cause tissue damage.
Product
INVUITY(R) PhotonBlade(TM), REF PB1
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2886-2017·2017-08-02
Peanut Butter Spread Recalled for Missing Coconut Allergen Labeling
Peanut Butter Holdings LLC is recalling PB Crave Coconut Milk Chocolate Peanut Butter Spread because the allergen statement fails to list coconut.
Product
PB Crave, Coconut Milk Chocolate Peanut Butter Spread, NET WT 16 OZ (1 LB) -454 g. Plastic jars, 6 per case.
Category
Food
Distribution
Distributed nationwide