Search by meaning, not just keywords: describe the product or the hazard and we find matching recalls even when the official notice uses different words. Brand names and model numbers work too.
Latest recalls
34,960 found- Use cautionMedical device
Nobel Biocare Usa Llc recalls NobelActive Internal NP 3.5x15mm Endosseus dental implant, REF: 34128, Rx Only, Sterile R, CE, UDI: (01)07332747010619
Nobel Biocare recalls 3.5x15mm Endosseus dental implants with potentially incorrect length labels that could cause nerve damage or extra surgery.
Nobel BiocareJul 19, 2019 - Lower riskMedical device
GE Healthcare, LLC recalls Aestiva 7900, Model Numbers: a) 1006-9300-000 b) 1006-9305-000 c) 1006-9118-000 d) 1006-9112-000 e) 1006-9113-000 f)
GE Healthcare recalls Aestiva 7900 anesthesia systems with specific model numbers due to cybersecurity vulnerabilities that could allow unauthorized flow sensor corrections when connected to hospital networks.
GE HealthcareJul 19, 2019 - Use cautionDrug
Ascend Laboratories LLC recalls Atorvastatin Calcium Tablet USP 80 mg, a) 90 count (NDC 67877-0514-90) and b) 500 count (NDC 67877-0514-05) bottles, Rx
Ascend Laboratories recalls specific lots of Atorvastatin Calcium Tablet USP 80 mg due to failed dissolution specifications. Check your bottle's NDC and lot number.
Ascend LaboratoriesJul 19, 2019 - Stop using nowDrug
Dercher Enterprises, Inc., DBA Gordon Laboratories recalls MONSEL'S (Ferric Subsulfate) Solution, 8 mL amber glass bottle, packaged as one dozen bottles with applicators per box,
Gordon Laboratories recalls 8 mL bottles of Monsel's Solution due to microbial contamination and incorrect iron content. Check your batch numbers.
Gordon LaboratoriesJul 19, 2019 - Lower riskDrug
Lupin Pharmaceuticals Inc. recalls Lisinopril and Hydrochlorothiazide Tablets USP, 20 mg/12.5 mg, 500-count bottle, Rx only, Manufactured for: Lupin
Lupin Pharmaceuticals recalls 500-count Lisinopril and Hydrochlorothiazide tablets due to foreign tablets found in product. Consumers should check if they have the specific lot number and contact the company for details.
LupinJul 19, 2019 - Lower riskFood
The Cookie Dough Cafe recalls The Cookie Dough Cafe - Chocolate chip chilled gourmet edible cookie dough; 1.6 oz bars, packaged in plastic wrappers,
The Cookie Dough Cafe recalls chocolate chip chilled edible cookie dough due to undeclared peanuts. This poses a risk for people with peanut allergies. Consumers should check product labels and contact the company for details.
The Cookie Dough CafeJul 19, 2019 - Stop using nowFood
Elevation Foods recalls Fresket egg salad packaged in 32oz plastic cup with lid, 2 cups per case, refrigerated
Elevation Foods recalls Fresket egg salad due to Listeria monocytogenes. Check your 32oz cups for lot code W1906042 and production date 12 AUG 2019A.
FresketJul 19, 2019 - Use cautionMeat & poultry
Koch Foods Recalls Breaded Poultry Products Due to Misbranding and Undeclared Allergens
USDA FSIS recalls 743 pounds of Koch Foods breaded chicken bites due to undeclared soy, milk, and egg allergens. Consumers urged to stop using these products immediately.
Koch FoodsJul 18, 2019 - Lower riskMedical device
Medical Intelligence Medizintechnik Gmbh recalls IGuide System, software versions: 2.2.0, 2.2.1, 2.2.2 Product Usage: Linear Accelerator. The intended use of the device
Medical Intelligence recalls iGuide System software versions 2.2.0, 2.2.1, and 2.2.2 for linear accelerators in radiotherapy. The software may incorrectly demand verification scans when the HexaPOD reaches target position, potentially causing positioning errors during treatment.
Medical IntelligenceJul 18, 2019 - Lower riskMedical device
Arrow International Inc recalls Arrow AGB+ Multi-Lumen CVC Kit-catheter permits venous access to central circulation by way of subclavian, jugular, and
Arrow recalls AGB+ Multi-Lumen CVC Kit (CDC-4270:1A) due to incorrect catheter length labeling. This may cause improper use in medical procedures. Contact Arrow for details.
ArrowJul 18, 2019 - Lower riskMedical device
Thermo Fisher Scientific (Monterrey) recalls Cardinal Health Brand 120mL/53mm sterile, individual peel pouch specimen container with orange cap (100/pk) Catalog
Cardinal Health recalls 100-pack sterile specimen pouches with orange caps due to potential plastic shavings inside. Consumers should check lot numbers listed in the recall notice.
Cardinal HealthJul 18, 2019 - Lower riskMedical device
Roche Diagnostics Operations, Inc. recalls cobas e 601 module (cobas 6000 Modular Series system) Part Number: 04745922001
Roche recalls cobas e 601 modules (part 04745922001) for potential inaccurate test results from a quality issue with high pressure solenoid valves.
RocheJul 18, 2019 - Stop using nowDrug
Baxter Healthcare Corporation recalls 0.9% Sodium Chloride Injection USP, 100 mL Viaflex Container, Rx Only, Baxter Healthcare Corporation, Deerfield, IL
Baxter Healthcare recalls 100mL 0.9% Sodium Chloride Injection (Rx Only) due to potential leakage in bags. Affected lots P389684 and P389742 expired 8/31/2020. Stop using if you have these items.
Baxter HealthcareJul 18, 2019 - Lower riskDrug
Ucb, Inc recalls Keppra (levetiracetam) 1000 mg tablets, 60 tablets per bottle, Rx only, Manufactured for UCB, Inc. Smyrna, GA 30080,
Ucb recalls Keppra 1000mg tablets with failed dissolution specifications. This may affect medication effectiveness. Return or stop using affected lots.
UcbJul 18, 2019 - Lower riskDrug
Amneal Pharmaceuticals, Inc. recalls Methylergonovine Maleate USP 0.2 mg Tablets a) 12 count (NDC 69238-1605-02) and b) 28 count bottles (NDC 69238-1605-08)
Amneal recalls Methylergonovine Maleate 0.2mg tablets due to foreign promethazine tablets found in some bottles. This could cause unintended medication effects if taken.
AmnealJul 18, 2019 - UnratedDrug
Preferred Pharmaceuticals, Inc recalls Neomycin Sulfate 3.5 mg/Polymyxin B Sulfate 10,000 units/Dexamethasone 1 mg Ophthalmic Ointment, Pkg Size 3 g Tube,
Preferred Pharmaceuticals recalls Neomycin Sulfate 3.5 mg/Polymyxin B Sulfate 10,000 units/Dexamethasone 1 mg ophthalmic ointment due to insufficient quality assurance controls in manufacturing. This product is available in specific lot numbers and expiration dates.
Preferred PharmaceuticalsJul 18, 2019 - Lower riskFood
Super Store Industries-Turlock Dairy Division recalls SUNNYSIDE FARMS PRESTIRRED PEACH YOGURT WITH OTHER NATURAL FLAVORS, 6 OZ (170g) CUP;99% Fat Free UPC# 7-17544-20293-6
Sunnyside Farms recalls peach yogurt with possible coconut contamination. Consumers should check UPC 7-17544-20293-6 for affected products. No action needed if not in the recall list.
Sunnyside FarmsJul 18, 2019 - Lower riskFood
Sunshine Bottling Co, Inc. recalls Sunchy Malta Pasteurized Non-Alcoholic Cereal Beverage in 7oz bottles 4 or 6/pack
Sunshine Bottling Co recalls Sunchy Malta Pasteurized Non-Alcoholic Cereal Beverage in 7oz bottles due to taste issues in specific lots. Consumers should check bottle caps for production date 06/28/2019.
Sunshine Bottling CoJul 18, 2019 - Lower riskFood
National Frozen Foods Corporation recalls Great Value Chopped Spinach, packed in poly bags, net wt. 12 oz. 12 oz. bag UPC: 0 78742 23740 4. master case UPC: 3 00
National Frozen Foods Corporation recalls Great Value Chopped Spinach (12 oz. bags) due to potential Listeria monocytogenes contamination. Consumers should check UPC codes and use by date for affected lots.
Great ValueJul 18, 2019 - Lower riskFood
Mountain Rose Inc. dba Mountain Rose Herbs recalls Fennel Whole Seed was packaged in a clear plastic bag or poly-woven bags sold in bulk form, net weight ranges from 4
Mountain Rose Herbs recalls fennel whole seed sold in clear plastic or poly-woven bags (4 oz to 50 lbs) due to potential Salmonella contamination. Consumers should check labels for lot #25031 and contact the company for details.
Mountain Rose HerbsJul 18, 2019 - Stop using nowConsumer product
Factory Direct Wholesale Recalls Folding Mattresses Due to Violation of Federal Mattress Flammability Standard
Factory Direct Wholesale recalls folding mattresses that fail federal flammability standards, risking fire. Consumers must stop using and return for free compliant cover.
Factory Direct WholesaleJul 18, 2019 - Stop using nowVehicle
VOLKSWAGEN CC (2016) recall — Air Bags
Volkswagen recalls 2015-2016 CC and Tiguan vehicles due to defective air bag ECUs that may deactivate or deploy unexpectedly. Free repair available.
VolkswagenJul 17, 2019 - Use cautionVehicle
PORSCHE 718 BOXSTER (2017) recall — Air Bags
Porsche is recalling certain 2017 Boxsters with air bag ECU defects that may cause deactivation or unintended deployment, increasing crash injury risk. Owners must contact Porsche for free software update and ECU replacement.
PorscheJul 17, 2019 - Use cautionVehicle
IC BUS CESB (2020) recall — Electrical System
Navistar recalls 2020 IC school buses with specific electrical systems due to risk of unintended engine starts during service. Owners must have repair completed by dealers to prevent injury.
NavistarJul 17, 2019 - Stop using nowMedical device
LABORIE MEDICAL TECHNOLOGIES, CORP recalls U3-3 Solar Blue, Laptop integrated power supply used with the Solar Blue Urodynamics for assessing lower urinary tract
Laborie Medical recalls Solar Blue Urodynamics power supplies due to fire risk from flammability issues. Affected units have specific serial numbers. Stop using immediately to prevent fire.
Laborie MedicalJul 17, 2019 - UnratedMedical device
Owen Mumford USA, Inc. recalls Autoject EI, REF AJ1310
Owen Mumford recalls Autoject EI (lot V14) due to possible assembly error. Affected units may have safety risks; contact for remedy.
Owen MumfordJul 17, 2019 - Lower riskMedical device
Becton Dickinson & Co. recalls Kit BD Max Enteric Viral Panel RUO; Catalog # 443715
Becton Dickinson recalls BD Max Enteric Viral Panel RUO kits with catalog #443715 due to foil bags not sealing properly. This could lead to contamination of reagents. Consumers should check product details and contact the company for instructions.
Becton DickinsonJul 17, 2019 - Lower riskDrug
Lupin Pharmaceuticals Inc. recalls Nystatin and Triamcinolone Acetonide Cream USP100,000 units/g, 0.1%, 15 g tube, Rx only, Manufactured for: Lupin
Lupin Pharmaceuticals recalls Nystatin and Triamcinolone Acetonide Cream due to failed content uniformity tests at 9 months. This may affect product stability and safety for patients using prescription medication.
LupinJul 17, 2019 - Lower riskDrug
Lupin Pharmaceuticals Inc. recalls Lisinopril and Hydrochlorothiazide Tablets USP, 10 mg/12.5 mg, 100 tablet bottle, Rx only, Manufactured by for: Lupin
Lupin Pharmaceuticals recalls 100-tablet bottles of Lisinopril and Hydrochlorothiazide tablets due to brownish/blackish stains and powder inside bottles. Affected products have NDC 68180-518-01 and batch H900575.
LupinJul 17, 2019 - Lower riskDrug
Macleods Pharma Usa Inc recalls Tamsulosin Hydrochloride Capsules, USP 0.4 mg Rx only a) 100 count (NDC 33342-159-11), b) 500 count (NDC 33342-159-15)
Macleods Pharma recalls 0.4 mg Tamsulosin capsules with failed dissolution specs. These prescription capsules may not work as intended. Contact for return instructions.
MacleodsJul 17, 2019
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