Official U.S. recalls · explained plainly

Know if it’s recalled — and exactly what to do.

We pull official government recall records and translate each one into plain language: what happened, how serious it is, and the steps to take. No legalese.

Search by meaning, not just keywords — describe the product or the hazard and we’ll find matching recalls even when the official notice uses different words. Brand names and model numbers work too.

Latest recalls

76,711 found

✓ Lower riskMedical device
Healthmark Industries Co., Inc. recalls healthmark ProChek-W Protein Test for Robotic Arms; ProChek-Semi Quantitative Protein Test, Model Number PT-SQ-001
Healthmark recalls ProChek-W and ProChek-Semi Quantitative Protein Tests with model PT-SQ-001 due to expired ingredients causing false negatives or positives. Serial numbers 200035-200040 and 30028 are affected.
HealthmarkJul 29, 2026
✓ Lower riskMedical device
Healthmark Industries Co., Inc. recalls healthmark ProChek-II, Model Number PT-313, PT-201-12
Healthmark recalls ProChek-II devices with specific serial numbers due to expired ingredients causing false test results. Affected units may show inaccurate results, potentially leading to incorrect health decisions.
HealthmarkJul 29, 2026
✓ Lower riskDrug
Shilpa Medicare Limited recalls PEMRYDI RTU(pemetrexed injection), 500 mg/50 mL (10 mg/mL), Single-dose vial, Rx only, Manufactured by: Zydus
Shilpa Medicare recalls PEMRYDI RTU (pemetrexed injection) due to green discoloration in vials. This may indicate contamination. Check vial color before use.
Shilpa MedicareJul 29, 2026
✓ Lower riskDrug
Shilpa Medicare Limited recalls PEMRYDI RTU (pemetrexed injection), 100 mg/10 mL (10 mg/mL), Single-dose vial, Rx only, Manufactured by: Zydus
Shilpa Medicare recalls PEMRYDI RTU (pemetrexed injection) vials with green discoloration. This may indicate contamination and should be discarded to avoid potential health risks.
Shilpa MedicareJul 29, 2026

Know if it’s recalled — and exactly what to do.

Latest recalls

Healthmark Industries Co., Inc. recalls healthmark ProChek-W Protein Test for Robotic Arms; ProChek-Semi Quantitative Protein Test, Model Number PT-SQ-001

Healthmark Industries Co., Inc. recalls healthmark ProChek-II, Model Number PT-313, PT-201-12

Shilpa Medicare Limited recalls PEMRYDI RTU(pemetrexed injection), 500 mg/50 mL (10 mg/mL), Single-dose vial, Rx only, Manufactured by: Zydus

Shilpa Medicare Limited recalls PEMRYDI RTU (pemetrexed injection), 100 mg/10 mL (10 mg/mL), Single-dose vial, Rx only, Manufactured by: Zydus

Apollo Care, LLC recalls SEMAGLUTIDE 5mg (1mg/mL), Glycine 25 mg (5mg/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection

Apollo Care, LLC recalls SEMAGLUTIDE 4.5mg (0.9 mg/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care,

Apollo Care, LLC recalls SEMAGLUTIDE 9mg (4.5 mg/mL), 2 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801

Apollo Care, LLC recalls SEMAGLUTIDE 10mg (5mg/mL), Glycine 10 mg (5mg/mL), 2 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection

Apollo Care, LLC recalls SEMAGLUTIDE 20mg (5mg/mL), Glycine 20 mg (5mg/mL), 4 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection

Prestige Brands Holdings recalls CLEAR EYES Maximum Itchy Eye Relief, 0.5 fl oz (15 mL) per dropper bottle, Sterile, Dist. by Medtech Products Inc.,

Apollo Care, LLC recalls SEMAGLUTIDE 0.9mg (0.9 mg/mL), 1 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care,

Apollo Care, LLC recalls SEMAGLUTIDE 6.75mg (4.5 mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care,

Apollo Care, LLC recalls SEMAGLUTIDE 2.5mg (1mg/mL), Glycine 12.5 mg (5mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous

Apollo Care, LLC recalls SEMAGLUTIDE 2.25MG (0.9 mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care,

Apollo Care, LLC recalls SEMAGLUTIDE 12.5MG (2.5MG/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care,

Apollo Care, LLC recalls SEMAGLUTIDE 7.5mg (5mg/mL), Glycine 7.5 mg (5mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous

Kerry, Inc recalls KC Everyday Mac & Cheese, 3lb x 6. Item # 20609055. 6 - 3 lb pouches, Net Wt: 18 lb. (8.16Kg). Fully Cooked. Keep

Regeneron Pharmaceuticals Inc recalls Libtayo (cemiplimab-rwlc) Injection, 350 mg/7 mL (50 mg/mL), For Intravenous Infusion After Dilution, Single-Dose Vial,

529 COMMERCE, LLC recalls Aquafaba Powder, Vegan Replacement, NET WT. 4 oz (113g) and 12 0z (340g), Resealable stand-up matte foil pouch with

FlavorsandColor.Com recalls Honeyville YELLOW COLOR 1 GALLON NFI: WATER, FD&C YELLOW #5, FD&C YELLOW #6, CITRIC ACID, AND SODIUM BENZOATE.

FORD F-250 SD (2023) recall — Back Over Prevention

Spectral Instruments Inc recalls Ami HTX

Spectral Instruments Inc recalls Lago X

American Regent, Inc. recalls Tralement (trace elements injection 4*, USP), packaged in a) 1mL Single Dose vials (NDC 0517-9305-01) and b) 5x1mL

Baxter Healthcare Corporation recalls Cefazolin in Dextrose, Injection, USP, 2g / 100mL (20mg / mL) Single-Dose Infusion Bag in 100mL GALAXY Plastic

American Regent, Inc. recalls Cyanocobalamin injection USP, 1,000 mcg/mL, For IM or SC Use Only, packaged in a) 1 mL Multi-Dose Vial (NDC

American Regent, Inc. recalls Selenious Acid Injection, USP 12 mcg/2 mL (6 mcg/2mL), For intravenous use, packaged in a) 2mL Single-Dose Vial (NDC

American Regent, Inc. recalls AMINAOCAPROIC ACID INJECTION, USP, 250 mg/mL (5 g/20 mL), packaged in a) 20 mL MULTIPLE DOSE VIAL FOR IV INFUSION (NDC

American Regent, Inc. recalls niCARdipine Hydrochloride Injection, USP, 25 mg/10mL (2.5 mg/mL), packaged in a) 10 mL Single Dose Vial (NDC

Mylan Pharmaceuticals Inc recalls Acamprosate Calcium, Delayed-Release Tablets, 333 mg, 180 tablets bottles, Rx only, Mylan Pharmaceuticals Inc.,