State

Northern Mariana Islands product recalls

73,372 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 73,372 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19226–19250 of 73395

ModerateFDA (Devices)·Z-1567-2022·2022-08-31
Stryker SWANSON Finger Joint Implant Incorrect Sizing Label on Carton
Wright Medical Technology is recalling 17 Stryker SWANSON Finger Joint Implants (size 00) due to incorrect sizing labels applied to carton packaging. Devices with lot numbers 1728375 and 1728376 were distributed across multiple US states and internationally.
Product
Stryker SWANSON Flexspan Finger Joint Implant W/O Grommets Silicone, Size: 00, REF 4700020, Sterile.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1405-2022·2022-08-31
Zarbee's Natural Children's Cough + Mucus Syrup Recalled for Storage Temperature Deviations
Family Dollar Stores is recalling Zarbee's Natural Children's Cough + Mucus syrup distributed April through June 2022 due to CGMP violations involving improper storage temperature conditions that may compromise product quality.
Product
ZARBEES NTRL CHLD COUGH MUCUS GRP 4 FL OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1635-2022·2022-08-31
Dynarex DynaLube Lubricating Jelly Recalled Due to Temperature Excursions
Mckesson is recalling Dynarex DynaLube lubricating jelly due to facility temperature excursions from June-August 2021 that may have degraded product effectiveness. Recall affects 17.5 boxes distributed nationwide between June-September 2021.
Product
DYNAREX DynaLube LUBRICATING JELLY, STR 2.7GM (144/BX 12BX/CS) Catalog #1250
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1414-2022·2022-08-31
Guardian Antacid Products Recalled Due to Improper Storage Conditions
Family Dollar's Guardian Antacid products were held outside appropriate storage temperatures, prompting an FDA Class II recall. Consumers should stop using affected products.
Product
GUARDIAN ANTACID EX STRGTH TBLT FRT 96CT SKU 901379 GUARDIAN CHWABLE SMTHIES BRRY FSION 60CT SKU 999845 GS EFFERVESCENT ANTACID TABLET 36 CT SKU 913102 GUARDIAN ANTCD TBLT XTRA STGTH BRY 96 CT SKU 914109 GUARDIAN ANTCID TBLT REG STTH FRT 150 CT SKU 914726 GC ANTACID…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1399-2022·2022-08-31
Cough Drops Recalled Due to Improper Storage Temperature Conditions
Family Dollar Stores is recalling Vicks VapoCool Drops and Best Health Honey Lemon Cough Drops due to CGMP deviations involving improper storage temperature conditions. No illnesses have been reported.
Product
VICKS VAPOCOOL DROPS SEVERE 18 CT SKU 999488 BEST HEALTH HONEY LEMON COUGH DROP 80 CT SKU 998844 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1403-2022·2022-08-31
MY CHOICE Levonorgestrel Tablets Recalled for Storage Temperature Deviation
Family Dollar Stores is recalling MY CHOICE Levonorgestrel Tablets due to storage temperature deviations that may affect product efficacy. The tablets were distributed nationwide between April 30 and June 10, 2022.
Product
MY CHOICE LEVONORGESTREL TABLET distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1603-2022·2022-08-31
DisCide Ultra Surface Disinfectant Recalled Due to Temperature Exposure
McKesson Medical-Surgical's DisCide Ultra Surface Disinfectant Cleaner is being recalled because temperature excursions may have reduced product effectiveness. The recall affects all lots distributed nationwide between June and September 2021.
Product
Palmero Healthcare, LLC DisCide Ultra Surface Disinfectant Cleaner Quaternary Based Manual Pour Liquid 1 gal. Jug Herbal Scent NonSterile Model Number: 3565G
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1393-2022·2022-08-31
Sleep aid products recalled due to improper storage temperature
Family Dollar sleep aid products were distributed outside proper temperature storage conditions. Consumers should stop using affected products and consult their healthcare provider if concerned.
Product
READY IN CASESLEEP AID SOFT GEL 32 CT SKU 901457 READY IN CASE SLEEP AID 64 CT SKU 999026 ZZZQUIL WARMING BERRY 12FL OZ SKU 999811 GOOD SENSESLEEP AID CAPLET 100 CT SKU 901496 GOOD SENSESLEEP AID CAPLET 24 CT SKU 913985 GOOD SENSE EZ NITE SLEEP BERRY 12FL OZSKU 999789…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1395-2022·2022-08-31
QP Motion Sickness Tablet 8 CT Recalled for Improper Storage Conditions
Family Dollar Stores is recalling QP Motion Sickness Tablet 8 CT (SKU 901583) packages distributed nationwide from April 30 to June 10, 2022, due to improper storage temperature conditions.
Product
QP MOTION SICKNESS TABLET 8 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1437-2022·2022-08-31
Blistex Lip Medex Recalled Due to Improper Storage Conditions
Family Dollar Stores is recalling specific Blistex Lip Medex products (SKUs 906120 and 998852) distributed April to June 2022 due to storage outside proper temperature conditions during distribution.
Product
BLISTEX LIP MEDEX 0.25OZ SKU 906120 BLISTEX LIP MEDEX POT 0.38 OZ SKU 998852 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1448-2022·2022-08-31
Bismuth-Based Antacids Recalled Due to Improper Storage Conditions
Multiple bismuth-based antacid products distributed by Family Dollar Stores are being recalled due to storage temperature deviations that violate manufacturing standards. No illnesses have been reported.
Product
GUARDIAN BISMUTH CHWBLE CHRY TABS 30 CTSKU 902321 RIC BISMUTH MAXIMUM STRENGTH 8 FL OZ SKU 914325 PEPTO BISMOL ORIGINAL 8 FL OZ SKU 914324 RIC BISMUTH REG STRENGTH CHERRY 8 FL OZ SKU 914781 PEPTO BISMOL CHERRY 8 FL OZ SKU 916063 PEPTO B LIQUID ORIGINAL TRAVEL 3.4 FL…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1576-2022·2022-08-31
Baxter Syringe Tip Caps Recalled Due to Sterile Packaging Barrier Failure
Baxter Healthcare is recalling DISCPAC Syringe Tip Caps due to potential packaging defects that may not maintain sterile barriers. The recall affects approximately 63,190 units distributed worldwide.
Product
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Orange: a) 25 pack, REF H93867025, b) 100 pack, REF H93867100
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1438-2022·2022-08-31
Carmex Lip Balm Products Recalled Due to Improper Storage Temperatures
Family Dollar Stores is recalling Carmex lip balm products (three SKUs) distributed from April 30 to June 10, 2022, due to CGMP deviations involving improper storage temperature conditions.
Product
CARMEX DAILY CARE CHERRY SPF 15 0.35 OZ SKU 901842 CARMEX LIP BALM JAR 0.25OZ SKU 903284 CARMEX STRWBRRY STCK W SPF 15 0.15OZ SKU 905760 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1453-2022·2022-08-31
Robitussin and Delsym Cough Medications Recalled for Storage Temperature Violations
Family Dollar Stores is recalling Robitussin Cough N Chest Congestion (4 FL OZ, SKU 919471) and Delsym Orange (3 FL OZ, SKU 901880) because these medications were stored outside proper temperature conditions.
Product
ROBITUSSIN COUGH N CHEST CONGESTION 4 FL OZ SKU 919471 DELSYM ORANGE 3 FL OZ SKU 901880 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1386-2022·2022-08-31
Three baby ointments recalled due to improper storage conditions
Three baby ointment products (Desitin Creamy, Baby Love, Desitin Maximum Strength) were recalled from Family Dollar Stores for being stored outside recommended temperature conditions. No illnesses or injuries have been reported.
Product
DESITIN CREAMY OINTMENT 2 FL OZ SKU 912976 BABY LOVE OINTMENT CREAM 4 OZ SKU 902617 DESITIN MAXIMUM STRENGTH PASTE 4 OZ SKU 903097 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1573-2022·2022-08-31
Mizuho OSI Femoral Hooks Recalled for Incorrect Model Etching
Mizuho OSI is recalling one batch of regular femoral hooks that were etched with an incorrect model designation. The recalled batch contains 13 devices distributed in the United States and Canada.
Product
HANA/PROFx CLASSIC FEMORAL HOOK RIGHT REF 6850-144
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1609-2022·2022-08-31
Medline Catheter Insertion Tray Recalled for Temperature Exposure During Manufacturing
Mckesson Medical-Surgical is recalling Medline catheter insertion trays (Model DYND10160) due to temperature excursions at the manufacturing facility that may have affected product effectiveness. Affected units were distributed nationwide between June and September 2021.
Product
MEDLINE INDUSTRIES Medline Catheter Insertion Tray Medline Foley Without Catheter Without Balloon Model Number: DYND10160
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1605-2022·2022-08-31
Hydrogen Peroxide Disinfectant Recalled for Potential Loss of Effectiveness
Revital-Ox Resert hydrogen peroxide disinfectant 4-liter containers may have reduced effectiveness due to temperature exposure during storage. McKesson is recalling affected lots distributed June-September 2021.
Product
STERIS CORP Revital-Ox Resert Hydrogen Peroxide High-Level Disinfectant Revital-Ox RESERT RTU Liquid 4 Liter Container Max 21 Day Reuse Model Number: 4455AW
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1392-2022·2022-08-31
Pain Reliever Caplets Recalled for Improper Storage Temperature
Over-the-counter pain reliever caplet products from Family Dollar stores are being recalled because they were stored outside proper temperature conditions.
Product
READY IN CASE PAIN RELIEVER PM CAPLET 100 CT SKU 902381 GOOD SENSE PAIN RELIEVER APAP 500MG CAPLET 250CT SKU 902332 READY IN CASE PM PAIN RELIEVER CAPLET 50 CT SKU 913982 GOOD SENSE PAIN RELIEVER APAP ES 500 CT SKU 999029 GOOD SENSE PAIN RELIEVER CAPLET 100 CT SKU 913890…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1627-2022·2022-08-31
Medical device swab recall: Fisherbrand SWAB TRANS STUARTS
Mckesson Medical-Surgical initiated a voluntary nationwide recall of Fisherbrand SWAB TRANS STUARTS swabs. The specific reason for the recall is not documented in the FDA notice.
Product
FISHER SCIENTIFIC Fisherbrand SWAB TRANS STUARTS DBL 50BX Catalog #1490721
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1616-2022·2022-08-31
B. Braun Anesthesia Support Tray Temperature Excursion Recall
B. Braun Medical Inc. is recalling Anesthesia Support Trays distributed between June and September 2021 due to temperature excursions during storage that may have affected product effectiveness.
Product
B. BRAUN MEDICAL INC. Anesthesia Support Tray SUPPORT TRAY, +EXT SET(10/CS)ST200E Model Number: 332116
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1397-2022·2022-08-31
FDA Recalls MICON Antifungal Drugs for Improper Storage Conditions
Family Dollar Stores is recalling READY IN CASE MICON 7 DAY and 3 DAY COMBO PACK products distributed April 30 through June 10, 2022, because they were stored outside appropriate temperature conditions. Consumers should stop using these products and return them to Family Dollar.
Product
READY IN CASE MICON 7 DAY 1.59 OZ SKU 939212 READY IN CASE MICON 3 DAY COMBO PACK SKU 902373 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1422-2022·2022-08-31
Ready In Case Isopropyl Alcohol Products Recalled for Storage Temperature Deviation
Family Dollar Stores is recalling Ready In Case rubbing alcohol and isopropyl alcohol products due to improper storage temperature conditions. The recall affects four SKUs distributed nationwide.
Product
READY IN CASE RUBBING ALCOHOL 91 PCT 16 FL OZ SKU 902270 READY IN CASE 70 PCT ISOPROPYL ALCOHOL 32 FL OZ SKU 999747 READY IN CASE 91PCT ISOPROPYL ALCOHOL 32 FL OZ SKU 999742 READY IN CASE 70PCT ISOPROPYL ALCOHOL 16 FL OZ SKU 999743 distributed to specific Family Dollar…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1373-2022·2022-08-31
Multiple ibuprofen products recalled for improper storage temperature
Family Dollar is recalling multiple ibuprofen products, including MOTRIN and GOOD SENSE brands, due to improper storage temperature conditions at distribution facilities from April through June 2022.
Product
MOTRIN IB CAPLETS 24CT SKU999394; GOOD SENSE IBUPROFEN 200MG TABLETS 24CT SKU 900556;GOOD SENSE IBUPROFEN 200MG CAPLET 50 CT SKU 902333 MOTRIN CHILDREN'S BUBBLEGUM 4 FL OZ SKU 903048 GOOD SENSE IBUPROFEN REGULAR SOFTGELS 160CT SKU 999373 GOOD SENSE IBUPROFEN 200 MG…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1622-2022·2022-08-31
Dynarex Nail Polish Remover Pads Recalled for Reduced Effectiveness from Heat Exposure
Mckesson Medical-Surgical Inc. is recalling Dynarex Nail Polish Remover Pads due to facility temperature excursions in summer 2021 that may have reduced product effectiveness. All lots received between June 1 and September 30, 2021, nationwide are affected.
Product
Dynarex¿ PAD, NAIL POLISH REMOVER (100/BX 10BX/CS) DYNREX Catalog # 1501
Category
Medical Device
Distribution
Distributed nationwide