Drug recalls, in plain English.
Recalled prescription and over-the-counter drugs, supplements and their FDA classification.
Recalls per year, by danger level
Drug recalls peaked in 2019 (1,788); 11,173 since 2017. 8% rated “stop using now”.
All FDA recall records in this category since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 44 | 38 | 164 | 895 | 1141 |
| 2018 | 61 | 40 | 258 | 1322 | 1681 |
| 2019 | 145 | 57 | 631 | 955 | 1788 |
| 2020 | 132 | 44 | 407 | 347 | 930 |
| 2021 | 96 | 44 | 562 | 450 | 1152 |
| 2022 | 97 | 56 | 611 | 626 | 1390 |
| 2023 | 108 | 59 | 402 | 553 | 1122 |
| 2024 | 65 | 39 | 243 | 210 | 557 |
| 2025 | 73 | 54 | 302 | 349 | 778 |
| 2026 (to date) | 70 | 60 | 238 | 266 | 634 |
Latest drug recalls
60 shown- UnratedDrug
Par Health USA, LLC recalls Argatroban Injection, USP, 250 mg/2.5mL (100 mg/mL), 2.5 mL x 1 Single Dose Vial, Rx only, Manufactured for: Endo USA,
Par Health USA, LLCOct 13, 2026 - UnratedDrug
Right Value Drug Stores LLC recalls Testosterone Cypionate, 200 mg/mL, packaged in a) 5 mL vials (NDC 73271-1225-1) and b) 30 m vials ( NDC 73271-1226-2)
Right Value Drug Stores LLCOct 9, 2026 - UnratedDrug
STRIDES PHARMA INC recalls Cinacalcet Tablets, 30 mg, 30-count bottle, Rx only, Manufactured by: Strides Pharma Science Ltd. Puducherry, 605 014,
STRIDES PHARMA INCOct 7, 2026 - UnratedDrug
Ascend Laboratories, LLC recalls Amlodipine and Olmesartan Medoxomil Tablets, 10mg/40mg, 30 Tablets, Rx only, Manufactured by: Alkem Laboratories Ltd.,
Ascend Laboratories, LLCOct 6, 2026 - UnratedDrug
Hikma Pharmaceuticals USA INC. recalls Abirtega (abiraterone acetate) USP, 250 mg, 120-count bottles, Rx only, Rx only, Mfd for: Hikma Pharmaceuticals USA
Hikma Pharmaceuticals USA INCOct 6, 2026 - Stop using nowDrug
American Health Packaging recalls Metoclopramide Tablets, USP, 5 mg, 100 Tablets (10 x 10), Rx Only, Distributed by: American Health Packaging, Columbus,
American Health Packaging recalls specific lots of Metoclopramide Tablets, USP, 5 mg due to the presence of foreign tablets or capsules.
American Health PackagingOct 6, 2026 - UnratedDrug
Greenwich Rx recalls Glutathione Injection (Glutathione-L, Ascorbic Acid, Sodium Hydroxide, Bacteriostatic Water), 200 mg/mL, 10 mL
Greenwich RxOct 1, 2026 - UnratedDrug
Viatris, Inc. recalls Telmisartan and Amlodipine, Tablets, USP, 40mg/5 mg, 30-count Bottle, Rx only, Manufactured for: Mylan Pharmaceuticals
Viatris, Inc.Oct 1, 2026 - UnratedDrug
Shenzhen Techdow Pharmaceutical Co., Ltd. recalls Heparin Sodium Injection, USP, 5,000 USP Units/mL, 1mL Multi dose vial x 25 vials per carton, Distributed by: Hepalink
Shenzhen Techdow Pharmaceutical Co., Ltd.Oct 1, 2026 - Use cautionDrug
Zydus Pharmaceuticals (USA) Inc recalls Hydrocortisone Sodium Succinate for Injection, USP 100 mg/vial, 1 Vial, Rx Only, Manufactured by: Zydus Lifesciences
Zydus recalls 70,776 vials of Hydrocortisone Sodium Succinate for injection due to failed impurity specifications. Check lot numbers LB00047A and LB00048A.
Zydus PharmaceuticalsOct 1, 2026 - UnratedDrug
Pfizer recalls Levoxyl (levothyroxine sodium tablets, USP), tablets, 175 mcg, 100 tablet bottle, Rx only, Distributed by Pfizer Inc.,
PfizerSep 29, 2026 - Use cautionDrug
Teva Pharmaceuticals USA, Inc recalls Metoclopramide Tablets, USP, 5 mg, [100 or 500] Tablets per bottle, Rx Only, Manufactured for: Teva Pharmaceuticals,
Teva Pharmaceuticals recalls specific lots of 5 mg Metoclopramide tablets due to the presence of foreign tablets and capsules. Check your bottle's lot number.
Teva PharmaceuticalsSep 29, 2026 - Use cautionDrug
Preferred Pharmaceuticals, Inc. recalls Lidocaine Ointment USP, 5% (Generic for Xylocaine), packaged in a 50 g jar, Rx only, Mfg: Taro Pharmaceuticals U.S.A.,
Preferred Pharmaceuticals recalls specific lots of Lidocaine Ointment USP 5% due to failed content uniformity specifications. Check your lot numbers.
Preferred PharmaceuticalsSep 28, 2026 - UnratedDrug
Houston Rx LLC recalls Sermorelin, 1 mg/mL, 10 ml vial, Sterile injectable solution, RX Only, Houston RX LLC, 15430 Vantage Parkway E STE 220,
Houston Rx LLC is recalling 7 vials of Sermorelin 1 mg/mL due to lack of process control. Check lot SER-081726-1-10 and beyond use date 10/01/2026.
Houston Rx LLCSep 25, 2026 - Use cautionDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Tretinoin Cream USP, 0.05%, 45 g tube, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured by: Taro
Northstar Rx LLC recalls specific lots of Tretinoin Cream USP 0.05% due to failed impurity specifications. Check your lot number immediately.
Northstar RxSep 25, 2026 - Stop using nowDrug
Apothecary Pharma LLC recalls Tirzepatide Injection, 18mg/mL, 4 mL Sterile Multi-Dose Vial, Rx only, Apothecary Pharma, LLC, 1913 Evans Road, Cary,
Apothecary Pharma LLC is recalling specific lots of Tirzepatide Injection vials due to a lack of assurance of sterility. Check your lot numbers immediately.
Apothecary PharmaSep 24, 2026 - Stop using nowDrug
J&J INNOVATIVE MEDICINE recalls IMAAVY (nipocalimab-aahu) Injection, 300 mg /1.62 mL (185 mg/mL) per single-dose vial, For Intravenous Infusion After
J&J recalls IMAAVY injection vials due to particulate matter. Check lot JNYJ1208, exp 10/30/2027 for details on this Class II drug recall.
J&J Innovative MedicineSep 23, 2026 - Use cautionDrug
Apotex Corp. recalls Paroxetine Extended-Release Tablets, 37.5mg, 30-count bottle, Rx only, Manufactured by: Apotex Inc., Toronto, Ontario,
Apotex Corp. recalls specific lots of Paroxetine Extended-Release Tablets, 37.5mg, because they failed dissolution specifications.
ApotexSep 23, 2026 - UnratedDrug
Cipla USA, Inc. recalls Fosfomycin Tromethamine Granules for Oral Solution, (Equivalent to 3 Grams of Fosfomycin), 1 Single-Dose Sachet, Rx
Cipla USA recalls specific lots of Fosfomycin Tromethamine Granules due to failed impurity specifications. Check your lot number and expiration date.
Cipla USASep 18, 2026 - Use cautionDrug
Ajanta Pharma USA Inc recalls Ranolazine Extended-Release Tablets, 1000 mg, 60-count bottle, Rx Only, Marketed by: Ajanta Pharma USA Inc.,
Ajanta Pharma USA Inc. recalls Ranolazine Extended-Release Tablets, 1000 mg, 60-count bottles due to failed dissolution specifications.
Ajanta PharmaSep 17, 2026 - Stop using nowDrug
Aurolab Trust recalls FOCUS PI Hypromellose 0.7% Formula, 0.3 FL O (10 mL) per vial, STERILE, Manufactured for: Covalent Management, Inc.,
Aurolab Trust recalls FOCUS PI Hypromellose 0.7% eye drops due to lack of sterility assurance. Check your batch numbers and expiration dates for affected units.
Aurolab TrustSep 17, 2026 - Lower riskDrug
Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company recalls Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye Drops (glycerin 0.25%, naphazoline hydrochloride 0.012%) with
Insight Pharmaceuticals recalls Clear Eyes Redness Relief eye drops due to lack of assurance of sterility. Affected lots may cause eye infections. Consumers should stop using and contact the company.
Insight PharmaceuticalsSep 15, 2026 - Use cautionDrug
K.C. Pharmaceuticals, Inc. recalls Sterile Lubricant Dry Eye Relief Eye Drops, 0.5 FL OZ (15 mL); a) LEADER, DISTRIBUTED BY CARDINAL HEALTH, DUBLIN, OHIO
K.C. Pharmaceuticals recalls over 1.3M cartons of dry eye relief drops due to lack of sterility assurance. Check your lot numbers and expiration dates.
Leader / TopCare / Crocodile TearsSep 11, 2026 - UnratedDrug
PRITAM INTERNATIONAL PRIVATE LIMITED recalls Brush Buddies, Mint Chocolate Chip Ice Cream Flavored Toothpaste, Anticavity Fluoride Toothpaste, (sodium fluoride
PRITAM INTERNATIONAL PRIVATE LIMITEDSep 10, 2026 - Stop using nowDrug
Carolina Infusion, LLC recalls QUAD-MIX( PAPAV/PHENTO/ALPROS/TROP) INJECTABLE, Packaged in single-use dosage syringes, total mL dispensed based on
Carolina Infusion LLC recalls specific lots of Quad-Mix injectable due to lack of sterility assurance. Check lot numbers and consult your provider.
Carolina InfusionSep 10, 2026 - Stop using nowDrug
Par Health USA, LLC recalls Buprenorphine Hydrochloride, Injection 0.3 mg/mL, Rx Only, 5 x 1 mL Single Dose Vials, Manufactured for: Endo USA,
Par Health USA recalls 154,210 bottles of Buprenorphine Hydrochloride Injection due to crystallization. Check lot numbers and expiration dates.
Par Health USASep 8, 2026 - Use cautionDrug
Amneal Pharmaceuticals, LLC recalls Estradiol Gel, 0.1%, 0.25 mg, 30-packets per carton, Rx only, Distributed by: Amneal Pharmaceuticals LLC, Bridgewater,
Amneal recalls Estradiol Gel packets due to defective containers that may be empty or partially full. Check your lot number and expiration date.
Amneal PharmaceuticalsSep 8, 2026 - UnratedDrug
Pfizer recalls Dopamine HCl Inj., USP, 200 mg/5 mL (40 mg/mL), 5 mL Single-dose, 25 vials per tray, Rx only, Distributed by Hospira,
Pfizer recalls 25-vial Dopamine HCl Injections due to lack of sterility assurance. This could lead to infections if used improperly. Affected products have specific NDC numbers and lot numbers.
PfizerSep 4, 2026 - Use cautionDrug
Inventia Healthcare Limited recalls Chlorthalidone Tablets, USP, 25 mg, 100 Tablets per bottle, Rx only, Manufactured by: Inventia Healthcare Limited. NDC:
Inventia Healthcare recalls 13,567 bottles of Chlorthalidone 25mg tablets due to failed dissolution specifications. Check your lot number and expiration date.
Inventia HealthcareSep 3, 2026 - Lower riskDrug
OurPharma LLC recalls fentaNYL Citrate, 1,000 mcg/100 mL (10mcg/mL) Injection solution in 100 mL, 0.9% NaCl Bag, OurPharma LLC, 2512 S. City
OurPharma LLC recalls fentanyl injection solution due to mismatched expiry dates on the IV bag and product. Affected units have a specific lot number and expiry date. Consumers should contact the manufacturer for details.
OurPharmaSep 3, 2026 - Use cautionDrug
SV Labs Toronto Corporation recalls Benzoyl Peroxide Wash, USP, 10%, packaged in a)5 FL OZ (148mL) bottles (NDC 0536-1261-63), and b) 8.5 FL OZ (237 mL)
SV Labs Toronto Corporation recalls specific lots of Benzoyl Peroxide Wash, USP 10% due to microbial contamination. Check your bottle's lot number and expiration date.
SV LabsSep 1, 2026 - Use cautionDrug
TerSera Therapeutics LLC recalls Zoladex (goserelin) implant, 3.6 mg, One single-Use Syringe packaged in a carton, Rx only, Manufactured for: TerSera
TerSera Therapeutics recalls 296 cartons of Zoladex 3.6 mg implants because they were exposed to uncontrolled temperatures during shipping.
TerSeraAug 31, 2026 - Lower riskDrug
SUN PHARMA /TARO recalls Lidocaine Ointment USP, 5%, Speermint Flavor, 50 g Jar, Rx only, Mfd. by: Taro Pharmaceuticals Inc., Brampton, Ontario,
SUN PHARMA /TARO recalls Lidocaine Ointment 5% (50g jar) due to failed content uniformity tests at 24 months. This may affect medication accuracy. Contact your pharmacy for details.
SUN PHARMA /TAROAug 31, 2026 - Lower riskDrug
Supernus Pharmaceuticals, Inc. recalls Trokendi XR, (topiramate) extended-release capsules, 50 mg, 30 Capsules, Rx only, Manufactured by: Catalent Pharma
Supernus Pharmaceuticals recalls Trokendi XR 50mg extended-release capsules due to failed dissolution specifications. This may affect safety and requires checking product details.
Supernus PharmaceuticalsAug 31, 2026 - Lower riskDrug
Amneal Pharmaceuticals of New York, LLC recalls Exenatide Injection, USP, 250 mcg/mL, 1.2 mL per prefilled pen, Rx Only, Subcutaneous Use Only, For Single Patient Use
Amneal recalls Exenatide injection pens that may contain no medication. This could lead to ineffective diabetes treatment. Check your pen's lot number and contact Amneal for details.
AmnealAug 28, 2026 - Lower riskDrug
Macleods Pharmaceuticals Limited recalls Olanzapine Tablets, USP 5 mg, 30-count bottle, Rx Only, Manufactured For: Macleods Pharma USA, Inc. Princeton, NJ,
Macleods Pharmaceuticals recalls 5mg Olanzapine tablets due to impurities that could pose health risks. Affected products have specific lot numbers and expiration dates. Consumers should contact the manufacturer for details.
MacleodsAug 27, 2026 - Lower riskDrug
Mylan Pharmaceuticals Inc recalls Carton label: Mycophenolate Mofetil for injection, USP, 500 mg/vial, Sterile, 4 Single Dose Vials, Rx only,
Mylan recalls 500mg Mycophenolate Mofetil injections due to failed dissolution specifications. Affected lots manufactured in India with specific NDC numbers and expiration dates. Patients should contact Mylan for details.
MylanAug 26, 2026 - Lower riskDrug
Ajanta Pharma USA Inc recalls Fluphenazine Hydrochloride Tablets, USP, 1mg, 100-count bottles, Rx Only, Marketed by: Ajanta Pharma USA Inc.,
Ajanta Pharma recalls 100-count Fluphenazine Hydrochloride tablets due to impurity levels exceeding safety limits. Affected lots have specific expiration dates and are prescription-only.
Ajanta PharmaAug 25, 2026 - Lower riskDrug
ImprimisRx NJ LLC recalls Povidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic Solution, 10 mL per dropper bottle, For Office Use Only,
ImprimisRx recalls 10mL ophthalmic solution with subpotent drug risk. This may not work as intended for eye procedures. Check NDC 71384-732-10 and lot numbers for affected products.
ImprimisRxAug 24, 2026 - UnratedDrug
Teva Pharmaceuticals USA, Inc recalls traZODone Hydrochloride Tablets, USP, 50 mg, Rx only, 100 Tablets, Manufactured in Croatia By: Pliva Hrvatska d.o.o,
Teva Pharmaceuticals recalls 50mg traZODone tablets manufactured in Croatia due to foreign tablets present. Consumers should contact Teva for details.
TevaAug 24, 2026 - UnratedDrug
Hikma Pharmaceuticals USA INC. recalls Ramipril Capsules USP, 10 mg, packaged in a) 100 Capsules (NDC 76282-673-01) and b) 500 Capsules (NDC 76282-673-05)
Hikma Pharmaceuticals recalls 10mg Ramipril capsules due to failed impurities test. Products may contain dicyclohexylurea (DCU) which could cause harm. Check NDC codes 76282-673-01 or 76282-673-05 for affected lots.
Hikma PharmaceuticalsAug 24, 2026 - Stop using nowDrug
VITRUVIAS THERAPEUTICS INC recalls Thyroid Tablets, USP, 1/2 Grain (30 mg), Each tablet contains: levothyroxine (T4) 19 mcg, liothyronine (T3) 4.5 mcg,
Vitruvias Therapeutics recalls thyroid tablets with superpotent drug levels. These tablets may cause serious health issues if taken without medical supervision.
Vitruvias TherapeuticsAug 21, 2026 - Use cautionDrug
Golden State Medical Supply Inc. recalls Prasugrel HCI, Tablets, USP, 10mg, 30-count bottle, Rx only, Marketed by: GSMS, Incorporated, Camarillo, CA 93012, USA,
Golden State Medical Supply recalls Prasugrel HCl 10mg tablets due to failed dissolution specifications. Check lot GS062298.
Golden State Medical SupplyAug 21, 2026 - UnratedDrug
Lexia LLC recalls Broadway Joe's Pain Cream, 3000 gm CBD, (Histamine Dihydrochloride 0.025%) (CDB Isolate 3000mg, HempSeed Oil 2000mg),4
Broadway Joe's recalls 3000g CBD pain cream due to potential raw material contamination. Affected lots expire January 2027. Consumers should check product labels for lot numbers.
Broadway Joe'sAug 21, 2026 - UnratedDrug
Sterling Pharmaceutical Services LLC recalls TRP The Relief Products* Gentle Eyes Lubricant Eye Drops, Carboxymethylcellulose sodium 0.5%, Sterile Eye Drops, 0.5 FL
Sterling Pharmaceutical Services LLC recalls TRP Gentle Eyes Lubricant Eye Drops due to lack of assurance of sterility. This could pose a risk of infection. Consumers should contact the manufacturer for details.
TRP The Relief ProductsAug 20, 2026 - Stop using nowDrug
B BRAUN MEDICAL INC recalls 0.9% Sodium Chloride Injection, USP, 100 mL Partial Fill in 150 mL PAB Container, Sterile, Rx only, B. Braun Medical
B. Braun Medical recalls 100mL sodium chloride injections with particulate matter (iron oxide, cellulose, polystyrene) in specific lots. Stop using if you have these lots.
B. Braun MedicalAug 19, 2026 - Lower riskDrug
Chiesi USA, Inc. recalls Revcovi (elapegademase-lvlr) Injection, 2.4mg/1.5mL (1.6 mg/mL), Single-Dose Vial, Rx Only, For Intramuscular Use Only,
Chiesi USA recalls Revcovi injection due to stability issues. The product may not maintain proper protein concentration. Affected units have specific lot numbers and expiration dates.
ChiesiAug 19, 2026 - Lower riskDrug
American Health Packaging recalls Buprenorphine Sublingual Tablets (C-III), 2 mg, 30 Tablets (3x10), Rx only, Distributed by: American Health Packaging,
American Health Packaging recalls 2mg Buprenorphine Sublingual Tablets (C-III) due to labeling mix-up. This may cause confusion with similar products. Check carton NDC 60687-481-21 for affected items.
American Health PackagingAug 19, 2026 - Lower riskDrug
Sage Products, LLC recalls 2% Chlorhexidine Gluconate* Cloth, Non-sterile, 6 Disposable cloths, Sage Products LLC, 3909 Three Oaks Road, Cary,
Sage Products LLC recalls 6-pack of non-sterile 2% chlorhexidine gluconate cloth due to cross contamination risk. Affected items have specific NDC and lot numbers.
Sage ProductsAug 18, 2026 - Lower riskDrug
Mylan Pharmaceuticals Inc recalls Prasugrel Tablets, USP, 10mg, Rx only, 30 Tablets in each bottle, Manufactured for: Mylan Pharmaceuticals Inc.,
Mylan recalls 10mg Prasugrel tablets that failed 18-month stability testing. These tablets may not be safe for long-term use. Consumers should contact Mylan for details.
MylanAug 17, 2026 - Stop using nowDrug
Baxter Healthcare Corporation recalls Dextrose Injection, USP, 70 %, 2000 mL bags, Rx Only, Baxter Healthcare Corporation Deerfield, IL, 60016, Made in USA,
Baxter recalls 2000mL dextrose injection bags with stainless steel particles. Stop using immediately due to potential serious injury from particulate matter in IV solutions.
Baxter HealthcareAug 17, 2026 - Stop using nowDrug
Baxter Healthcare Corporation recalls 0.9% Sodium Chloride Injection USP 500 mL, VIAFLEX Plastic Containers, with 24 units per case. Baxter Healthcare
Baxter recalls 500mL saline injections in VIAFLEX plastic containers due to fiberglass particulates. Stop using if you have these containers with specific lot numbers.
Baxter HealthcareAug 17, 2026 - Lower riskDrug
Allies Group Inc. recalls THE ONE SPF 50 INVISIBLE SUNSCREEN GEL, (Avobenzone 3%, Homosalate 7%, Octocrylene 10%, Octisalate 5%), 20ml - 0.7 fl.
Allies Group recalls The One SPF 50 Invisible Sunscreen Gel (20ml) that may not provide reliable SPF 50 protection. Consumers should check product details and contact Allies Group for guidance.
Allies GroupAug 14, 2026 - Lower riskDrug
Safecor Health, LLC recalls Fluphenazine HCl Elixir, USP, 2.5 mg per 5 mL, Delivers: 5 mL, Oral Elixir, PAI, Alcohol 14% by volume, For Oral Use
Safecor Health recalls Fluphenazine HCl Elixir due to failed stability specifications. This medication may degrade over time, potentially affecting safety. Consumers should check product details and contact the manufacturer for instructions.
Safecor HealthAug 13, 2026 - Lower riskDrug
Apotex Corp. recalls Paxil CR, Paroxetine, Extended-Release Tablets, 37.5mg, 30 count bottle, Rx only, Manufactured by: Apotex Inc.,
Apotex recalls 37.5mg Paxil CR tablets due to failing 24-month stability tests. This may affect medication safety. Check your prescription bottle for NDC 60505-4379-3.
ApotexAug 13, 2026 - UnratedDrug
B BRAUN MEDICAL INC recalls Lactated Ringer's Injection USP, 1000 mL EXCEL container, Rx only, L7500, B. Braun Medical, Inc., Bethlehem, PA
B. Braun Medical recalls Lactated Ringer's Injection USP 1000mL (L7500) due to particulate matter. Affected units have specific lot numbers and expiration dates. Consumers should contact the manufacturer for details.
B. Braun MedicalAug 12, 2026 - Stop using nowDrug
American Regent, Inc. recalls Epinephrine Injection, USP, 30 mg/30 mL (1mg/mL), 30 mL-Multiple-Dose Vial, Rx Only, For Intravenous Infusion,
American Regent recalls epinephrine injections with particulate matter and lack of sterility. Affected lots expire August 2026 through July 2027. Stop using immediately if you have these vials.
American RegentAug 11, 2026 - Stop using nowDrug
Fresenius Kabi USA, LLC recalls Tyenne (tocilizumab-aazg) Injection, 400 mg/20 mL (20 mg/mL), 20 mL vial, Rx Only, Manufactured by Fresenius Kabi USA,
Fresenius Kabi recalls Tyenne (tocilizumab-aazg) injection due to glass particles found in some batches. This may cause serious injury if injected. Affected units have specific lot numbers and expiration dates.
Fresenius KabiAug 10, 2026 - Lower riskDrug
Church & Dwight Co., Inc. recalls Zicam, Cold Remedy, Medicated Nasal Swabs, With Cooling Menthol & Eucalyptus, 20 Single-Use Swabs per carton, Zinc-Free
Church & Dwight recalls Zicam Cold Remedy nasal swabs due to microbiological testing failures found during FDA inspection. Affected lots have specific expiration dates and UPC codes.
Church & DwightAug 10, 2026 - UnratedDrug
SHANTOU Qiwei industrial Co., Ltd recalls MENOW SUNSCREEN PRESSED POWDER SPF35 PA+++, Net content, 9g/0.32 oz, Manufactured by: Shantzu Qiwei Industry Co. Ltd,
MENOW SPF35 pressed powder sunscreen with lot #2024/10/11 is recalled due to cGMP deviations. Consumers should check product details and contact the manufacturer for instructions.
MENOWAug 8, 2026