State

Maine product recalls

73,388 recalls have nationwide distribution and so reach Maine. 3,922 additional recalls listed Maine specifically in their distribution scope.

What the numbers show

Total: 3,922
Critical: 478
Severe: 964
Most recent: 2026-09-23

Of the 3,922 recalls naming Maine we have scored against our rubric, 478 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 964 (25%) are Severe.

Which agencies issued them

These figures cover only the 3,922 recalls whose distribution notice names Maine specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19926–19950 of 77310

ModerateFDA (Drugs)·D-1378-2022·2022-08-31
Antibacterial Wipes Recalled for Improper Storage Conditions
Family Dollar Stores recalls Disney Licensed Anti Bac Wipes and Antibacterial Wipes due to storage temperature deviations. The products were distributed nationwide to Family Dollar stores from April 30 through June 10, 2022.
Product
DISNEY LICENSED ANTI BAC WIPES 20 CT SKU 998908; ANTIBACTERIAL WIPES 40CT SKU 2007538 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1569-2022·2022-08-31
Anatomical Model Recalled for Wrong Product Shipped in Packaging
Materialise USA LLC is recalling ProPlan CMF Anatomical Model units where packages labeled MU22-INA-DUQ contained the wrong anatomical model inside. Recipients should verify their package contents match the label.
Product
ProPlan CMF Anatomical Model, Maxilla-Cranium, Clear Identification number SD900.208
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1456-2022·2022-08-31
OTC Cough Medications Recalled for Improper Storage Temperature
Family Dollar is recalling four OTC cough and mucus relief medications that were stored outside appropriate temperature conditions.
Product
REFENESEN MUCUS RELIEF TABLET 30 CT SKU 917531 MUCINEX DM MAX STRENGTH 7CT SKU 900854 RIC MUCUS RLF DM MAX STNGTH CHRY 6FL OZ SKU 999559 VICKS JARABE COUGH CONGESTION 8FLOZ SKU 998933 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1394-2022·2022-08-31
Medicated chest rubs recalled for improper storage temperature conditions
Vicks VapoRub and Swan Medicated Chest Rub products from Family Dollar Stores are being recalled due to improper storage temperature conditions during their distribution.
Product
VICKS VAPORUB 1.76 OZ SKU 919667 VICKS VAPOR RUB LAVENDER 1.76 OZ 999813 SWAN MEDICATED CHEST RUB 3.53 OZ SKU 920611 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1369-2022·2022-08-31
Hydrogen Peroxide Recalled Due to Improper Storage Conditions
Family Dollar Stores is recalling Hydrogen Peroxide 16 oz. and 32 oz. bottles distributed from April 30 to June 10, 2022 due to storage outside required temperature ranges. Products have SKUs 909221 and 901675.
Product
Hydrogen Peroxide 16 fl. oz. and 32 oz. bottles distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1634-2022·2022-08-31
Dynarex Lemon Glycerin Swabs recalled due to temperature exposure
Dynarex lemon glycerin swabs distributed nationwide may have reduced effectiveness due to temperature excursions prior to delivery. All lots received between June 1 and September 30, 2021 are affected.
Product
Dynarex SWAB, LEMON GLYCERIN (3/PK 25PK/BX 10BX/CS) DYNREX Catalog # 1216
Category
Medical Device
Distribution
Distributed nationwide
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