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
34,896 found- Use cautionMedical device
Intersurgical Inc recalls Flexible Smoothbore Breathing Circuit with Exhalation Port 22mm, Product No. 80062000
Intersurgical recalls flexible breathing circuits with exhalation port 22mm due to risk of blocking during assembly, potentially causing serious patient health issues. Affected units include specific product numbers listed in the recall.
IntersurgicalApr 25, 2018 - Lower riskMedical device
Conseal International, Inc. recalls Nanosil Spray Gel, "***IMMUNE SYSTEM SUPPORT***ENGINEERED NANO-SILVER SOLUTION***", Net. Wt. 4 fl. oz./118mL, Catalog
Conseal International recalls Nanosil Spray Gel due to missing lot codes and expiration dates, posing risks from unverified manufacturing practices. Consumers should check product labels for these identifiers.
ConsealApr 25, 2018 - Lower riskMedical device
ConvaTec, Inc recalls Convatec Esteem(TM) Synergy Stomahesive(R), 7/8 in. / 22mm, REF 405475 Product Usage: Esteem Synergy Stomahesive with
ConvaTec recalls Esteem Synergy Stomahesive skin barrier wafers with a larger stoma hole than labeled, which may cause improper fit and discomfort for ostomy users.
ConvaTecApr 25, 2018 - Lower riskMedical device
Baxter Healthcare Corporation recalls Baxter EXACTAMIX Inlet, Vented, High-Volume Inlet, REF H938174 Usage: Exacta-Mix 2400 Compounding System Administration
Baxter recalls specific EXACTAMIX Inlet models due to incorrect labeling that may lead to expired product use. Affected lots include 802279, 802: 802280, 802281.
BaxterApr 25, 2018 - Lower riskFood
A G Specialty Foods, Inc. recalls Zoi Mixed Berry Greek Yogurt Parfait, 9 oz. clear plastic cup, covered with a clear plastic snap-on lid. UPC 8 17203
A G Specialty Foods recalls Zoi Mixed Berry Greek Yogurt Parfait due to coconut not being listed in the Contains statement. Check UPC 8 17203 for affected lots.
ZoiApr 25, 2018 - Use cautionFood
Wysong Corporation recalls Protein key brand Protein Meals varieties, 2.5 lb plastic container and 400 g plastic container, Varieties: Essentials
Wysong recalls Protein Key meals with undeclared soy allergen. All products with lot codes 042016-042018 in 2.5lb or 400g containers are affected. Consumers should check labels for soy content.
WysongApr 25, 2018 - Stop using nowConsumer product
HD Supply Recalls Ceiling Fans Due to Impact Hazard (Recall Alert)
HD Supply recalls Seasons 52" ceiling fans with bracket failure risk. Stop using immediately to prevent blade falls.
SeasonsApr 25, 2018 - Use cautionVehicle
HYUNDAI IONIQ HYBRID (2017) recall — Hybrid Propulsion System
Hyundai recalls 2017 Ioniq Hybrid vehicles with potential electrical short causing fire. Owners must have HCA caps inspected for oil leaks and replaced if needed. Free fix starts June 20, 2018.
HyundaiApr 24, 2018 - Use cautionVehicle
BLUE BIRD VISION (2017) recall — Vehicle Speed Control
Blue Bird is recalling 2017-2018 Vision buses with Gen4 Ford engines due to potential brake and throttle interlock failure, risking unexpected bus movement and crashes.
Blue BirdApr 24, 2018 - Use cautionVehicle
BLUE BIRD VISION (2017) recall — Vehicle Speed Control
Blue Bird is recalling 2017-2018 Vision school buses with Gen4 Ford engines that may move unexpectedly due to brake/throttle issues. Owners must contact Blue Bird for software update.
Blue BirdApr 24, 2018 - Lower riskMedical device
Biocare Medical, LLC recalls Vulcan Fast Red Chromogen Kit 2, part of an immunohistochemistry (IHC) procedure using an alkaline phosphatase (AP)
Biocare Medical recalls Vulcan Fast Red Chromogen Kit 2 (FR805-5L, FR805S) due to stability issues with raw materials causing chromogen failure in IHC procedures.
Biocare MedicalApr 24, 2018 - Lower riskMedical device
Medtronic Inc. recalls Medtronic MiniMed Paradigm Veo Insulin Pump Product Catalog Number: MMT-554, MMT-754
Medtronic recalls MiniMed Paradigm Veo insulin pumps with catalog numbers MMT-554 and MMT-754 that have an Arabic language translation error in the Predictive Alerts setting screen. This error may cause incorrect alerts for low or high glucose levels.
MedtronicApr 24, 2018 - Lower riskMedical device
Medline Industries Inc recalls MEDLINE Sterile* Needle Counter, 40Ct. Foam Block / Adhesive, reorder: DYNJNC40A Product Usage: A needle counter is
Medline recalls sterile needle counters with potential packaging seal issues that could compromise sterility. Affected lots include 67016114501-67017104502. Consumers should check their product lot numbers.
MedlineApr 24, 2018 - Lower riskMedical device
Baxter Healthcare Corporation recalls Prismaflex 7.20 US, Product Code 955542 Intended Use: The Prismaflex Control Unit is intended for: " Continuous Renal
Baxter recalls Prismaflex 7.20 US control units with product code 955542 due to potential firmware failure causing device inoperability. Affected units may require firmware update to prevent voltage issues.
BaxterApr 24, 2018 - Use cautionDrug
Mylan Pharmaceuticals Inc. recalls Loxapine Capsules, USP 50 mg, Rx Only, 100-count bottles, NDC 0378-7050-01
Mylan Pharmaceuticals recalls 11,650 bottles of Loxapine Capsules USP 50 mg due to Current Good Manufacturing Practice deviations. Check your lot numbers.
Mylan PharmaceuticalsApr 24, 2018 - Lower riskDrug
Mylan Pharmaceuticals Inc. recalls Amlodipine and Benazapril HCL Capsules, USP, 5 mg/40 mg, 100 count bottles, Mylan Pharmaceuticals, Inc., Morgantown, WV
Mylan recalls 100-count Amlodipine and Benazapril capsules due to cleaning process deviations in manufacturing. Products with specific NDC and lot numbers are affected.
MylanApr 24, 2018 - Stop using nowDrug
Vitalab Pharmacy, Inc recalls Methylcobalamin for injection, 1mg/mL and 10 mg/mL, Sterile injectable, Vitalab Pharmacy, Inc
Vitalab Pharmacy recalls Methylcobalamin for injection due to lack of sterility assurance. Check lot numbers and expiration dates if you have this drug.
Vitalab PharmacyApr 24, 2018 - Lower riskDrug
Prescript Pharmaceuticals, Inc. recalls Acetaminophen 300 mg with Codeine Phosphate 30 mg tablets, USP, 20-count M-Pak containers, Rx Only. Mnfct for:
Prescript Pharmaceuticals recalls 20-count acetaminophen with codeine tablets due to incorrect storage temperature label. The product should be stored at 20°C to 25°C (68°F to 77°F), not 15°C to 30°C (59°F to 86°F).
Prescript PharmaceuticalsApr 24, 2018 - Lower riskFood
Labrada Nutrition, Inc recalls Lean Pro 8 Chocolate 2,268g (5lb) Tub and Lean Pro 8 Chocolate 1,000g (2.2lb) Tub
Labrada Nutrition recalls two chocolate tub sizes due to undeclared egg in product. Consumers should check lot numbers and UPCs listed to determine if affected.
Labrada NutritionApr 24, 2018 - Stop using nowFood
Greenbelt Greenhouse Ltd recalls Fresh Microgreen Mix, Greenbelt Microgreens brand, net wt. 75 gram. Product is packaged in a clear plastic clam shell
Greenbelt Greenhouse Ltd recalls 75g Fresh Microgreen Mix due to potential Listeria monocytogenes contamination. Check your package dates and UPC.
Greenbelt MicrogreensApr 24, 2018 - Stop using nowConsumer product
Honeywell Recalls Hard Hats Due to Risk of Head Injury
Honeywell recalls Fibre-Metal E2 and North Peak A79 hard hats due to potential head injury risk. Affected models have specific manufacture dates and mold numbers. Consumers should stop using and get credit.
HoneywellApr 24, 2018 - Lower riskMedical device
DeRoyal Industries Inc recalls DeRoyal(R) SURGI MATE(R) Electrosurgical Pencil, Button Switch, with 15 ft (4.6 m) Cord and Holster, REF 88-001502
DeRoyal recalls SURGI MATE electrosurgical pencils with non-sterile packaging. This could lead to infection during surgery if used without proper sterilization.
DeRoyalApr 23, 2018 - Lower riskMedical device
Intuitive Surgical, Inc. recalls da Vinci Xi EndoWrist Stapler 45 Reload Green, Model 48445G-03, 12 reloads/box.
Intuitive Surgical recalls da Vinci Xi EndoWrist Stapler 45 Reload Green (Model 48445G-03) due to potential missing knife component causing failure to cut tissue. Affected units sold until 2020.
Intuitive SurgicalApr 23, 2018 - Stop using nowMedical device
Tandem Diabetes Care Inc recalls t:slim G4 Insulin Pump with Dexcom G4 Platinum CGM Software version: 4.3.4.3, Firmware version: 004722, Firmware, Fuel
Tandem recalls 55 t:slim G4 insulin pumps due to faulty fuel gauges that may cause inaccurate battery readings and stop insulin delivery.
Tandem Diabetes CareApr 23, 2018 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Metoprolol Succinate Extended-Release Tablets, USP, 100 mg, 100 Tablets bottle, Rx only, Manufactured by: Dr. Reddy's
Dr. Reddy's recalls 100-mg Metoprolol Succinate Extended-Release Tablets due to foreign Clopidogrel tablets found in some bottles. This is a prescription-only product.
Dr. Reddy'sApr 23, 2018 - UnratedDrug
Mckesson Packaging Services recalls Diltiazem CD (Diltiazem Hydrochloride Extended-Release Capsules, USP) 180 mg, 100-count bottles, Rx Only Mfg. By:
Mckesson recalls 180mg Diltiazem CD capsules with failed dissolution testing. This may cause inconsistent drug release. Check NDC 63739-284-10 and lot 0114214 for affected products.
Mckesson Packaging ServicesApr 23, 2018 - Lower riskFood
Ziegenfelder Company, Inc. recalls Budget $aver Monster Cherry-Pineapple Pops Net Contents 36 FL OZ
Ziegenfelder recalls Budget $aver Monster Cherry-Pineapple Pops due to Listeria monocytogenes found in Denver plant samples. Consumers should check lot codes D09418A-D10018B for affected products.
ZiegenfelderApr 23, 2018 - Use cautionFood
HEALTHY FOOD INGREDIENTS recalls Great Value Organic Ground Flax Seed, Net Wt. 16 oz. (1 LB) 454g. UPC 78742-14161, and Net Wt. 32 oz. (2 LB) 907g, UPC
Great Value Organic Ground Flax Seed (16oz & 32oz) may contain metal fragments. Consumers should stop using and return items to Wal-Mart for replacement.
HEALTHY FOOD INGREDIENTSApr 21, 2018 - Lower riskMedical device
LivaNova USA recalls Sorin Stockert Heater-Cooler System 3T, a) Item #: 16-02-81, 240 v/60 Hz; b) Item #: 16-02-82, 208 v/60 Hz; c) Item #:
LivaNova recalls Sorin Stockert Heater-Cooler System 3T units with specific item and serial numbers due to suspected microbial contamination and visible biofilm. Affected units may require cleaning or replacement.
LivaNovaApr 20, 2018 - Use cautionMedical device
CareFusion 303, Inc. recalls Alaris Infusion Pump administration sets labeled as: -Infusion Set Alaris Pump Module/Medley Pump Module/Gemini
CareFusion recalls Alaris infusion pump sets that users cannot prime. These sets may cause fluid flow issues. Stop using immediately to prevent potential complications.
CareFusionApr 20, 2018
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