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
34,893 found- UnratedMedical device
Aesculap Implant Systems LLC recalls JS Series SterilContainer S2 System
Aesculap recalls JS Series SterilContainer S2 Systems sold without FDA 510K clearance. These surgical containers may pose risks due to lack of regulatory approval before market release.
AesculapSep 8, 2017 - Lower riskMedical device
Sysmex America, Inc. recalls Sysmex Fluorocell(R) PLT Fluorocell PLT is used to stain platelets in a diluted blood sample for the counting of
Sysmex America recalls Fluorocell PLT test kits with lot numbers A6051-A6090. These kits may cause false low platelet results, leading to inaccurate blood test counts. Affected users should check for error messages in their Sysmex XN-Series analyzers.
SysmexSep 8, 2017 - Lower riskMedical device
Limacorporate S.p.A recalls Delta Cup Beater Positioner - Aligner, model # 9057.20.555 Used during implantation of the Delta Acetabular System
Limacorporate recalls Delta Cup Beater Positioner model 9057.20.555 used in hip implants due to potential weakness from suboptimal welding. Affected units include specific lot numbers sold in 2014-2016.
LimacorporateSep 8, 2017 - Use cautionMedical device
Handicare Usa Inc recalls PRISM MEDICAL A-625, MAX. LOAD 625 lbs. 283 Kgs., Patient lift, non-A/C powered
Handicare recalls A-625 patient lifts made between April 2017 and June 2017 due to potential strap wear at max load (625 lbs) that could cause patient drop. Affected units have specific serial numbers.
HandicareSep 8, 2017 - Use cautionMedical device
Howmedica Osteonics Corp. recalls AccuLIF TL Insertion Handle The AccuLIF Insertion Handle attaches to the implant and is specifically designed to allow
Howmedica recalls AccuLIF TL Insertion Handle model 800804 with lot numbers 160010 and 170003 due to potential implant pivot during surgery. Affected patients should contact Howmedica for details.
HowmedicaSep 8, 2017 - Lower riskDrug
AbbVie Inc. recalls AndroGel (testosterone gel) 1.62%, 40.5mg in 2.5g aluminum foil packet, 30 Packets per carton. Rx Only. Marketed by:
AbbVie recalls 30-packs of AndroGel testosterone gel (1.62%, 40.5mg) for prolonged exposure to improper temperatures. This may affect safety if stored outside labeled conditions.
AbbVieSep 8, 2017 - Lower riskFood
Bravo Produce Inc recalls Maradol Papaya; Frutas Selectas De Tijuana, S. DE R.L. DE, C.V. Sold in 14.00 kg/ 31 Lb. cardboard boxes.
Bravo Produce is recalling Maradol Papaya due to Salmonella contamination. Products sold in 14kg cardboard boxes may cause foodborne illness. Consumers should avoid eating these items.
Bravo ProduceSep 8, 2017 - Lower riskFood
SIMPLY FRESH FOODS INC recalls San Francisco Foods Seafood Salad; Deli Style Seafood Salad with Greek Yogurt; 4 x 4 oz. (113 g) cups Net Wt. 16 oz.
Simply Fresh Foods recalls seafood salads with possible incorrect milk labeling. Products may not properly declare milk as an allergen. Consumers should check UPC codes and use by dates.
Simply Fresh FoodsSep 8, 2017 - Lower riskFood
Apple King, LLC recalls Fuji apples, Nature's Delight brand, packaged in tray pack box size 64, net weight 40 lbs., PLU 4131, distributed by
Nature's Delight Fuji apples (40 lbs, PLU 4131) recalled due to Thiabendazole detected at 6.9 ppm. Consumers should avoid these apples.
Apple KingSep 8, 2017 - Use cautionConsumer product
Nantucket Distributing Recalls Patio Set Chairs Due to Fall Hazard
Nantucket Distributing recalls Bimini patio chairs with fabric seats that can tear, causing fall hazards. Consumers must stop using and return chairs for refunds via Christmas Tree Shops.
Nantucket DistributingSep 8, 2017 - Lower riskMedical device
Zimmer Biomet, Inc. recalls The 2nd Assist Knee Positioner
Zimmer Biomet recalls The 2nd Assist Knee Positioner (Item# 740026) due to potential sterile packaging breach during distribution. Affected medical devices may not be sterile.
Zimmer BiometSep 7, 2017 - Lower riskMedical device
Radiometer America Inc recalls AutoCheck5+, Level 2, specifically designed for Radiometer Americas blood gas analyzers The QUALICHECK+ quality
Radiometer America recalls AutoCheck5+ Level 2 QC ampoules for blood gas analyzers that may give incorrect pCO2 and pO2 results. Affected units were sold with specific lot numbers.
Radiometer AmericaSep 7, 2017 - Use cautionFood
Garden Of Life, LLC recalls Garden of Life, Baby Organic Liquid probiotic formula, 56 ml (1.9 fl oz)
Garden of Life recalls Baby Organic Liquid probiotic formula (56ml) due to choking risk for newborns. Check lot numbers 5487617-550087 for affected products.
Garden of LifeSep 7, 2017 - Lower riskFood
Good Eggs SF - Bay recalls Panang Curry included in the Beef Panang Curry Dinner, 3.5 oz. 8oz plastic deli container bearing the name Curry Paste.
Good Eggs SF Bay recalls Panang Curry dinner due to peanuts not listed as an allergen despite being an ingredient. This poses a risk for those with peanut allergies.
Good Eggs SF - BaySep 7, 2017 - Stop using nowConsumer product
Studio Fun International Recalls Slap Bracelets Sold with Children's Storybooks Due to Laceration Hazard
Studio Fun International recalls slap bracelets sold with DreamWorks Trolls storybooks due to laceration hazards from exposed metal bands.
Studio Fun InternationalSep 7, 2017 - Stop using nowConsumer product
Smith Recalls Ski and Snowboard Helmets Due to Risk of Head Injury
Smith recalls 2016-2017 Quantum ski and snowboard helmets due to buckle disengagement risk. Affected models sold in matte colors with internal label showing manufacturing dates.
SmithSep 7, 2017 - Stop using nowConsumer product
L.L. Bean Recalls Toddler Sweater Fleece Pullovers Due to Choking Hazard (Recall Alert)
L.L. Bean recalls toddler fleece pullovers with detachable snaps that pose a choking hazard. Affected items sold in 2T, 3T, 4T sizes with blue trim and specific colors. Consumers should stop using and get a refund.
L.L. BeanSep 7, 2017 - Use cautionMedical device
Biosense Webster, Inc. recalls THERMOCOOL SF NAV Catheters Model Numbers - BNI35FJCT, BNI35DFCT, D-131503-S, D-131504-S
Biosense Webster recalls THERMOCOOL SF NAV catheters with specific model numbers due to Alert 402 causing potential unintended ablation areas during cardiac procedures.
Biosense WebsterSep 6, 2017 - Lower riskFood
Coborn's, Inc recalls Coborn's/Cash Wise Caraway Rye Bread - UPC 7-33147-20155-8 Net Wt. 16 oz (1.0 lb) (454 g) Sell by 9/6/2017
Coborn's recalls Caraway Rye Bread (UPC 7-33147-20155-8) due to incorrect allergen labeling. The product lists wheat, milk, egg and soy instead of just wheat, posing a risk for those with allergies to those ingredients.
Coborn'sSep 6, 2017 - Stop using nowConsumer product
Kawasaki Recalls Brute Force 300 All-Terrain Vehicles Due to Fire Hazard
Kawasaki recalls 2012-2017 Brute Force 300 ATVs due to fuel leaks that could cause fire. Owners must stop using and contact for free repair.
KawasakiSep 6, 2017 - Stop using nowConsumer product
Ameriwood Home Recalls Chests of Drawers Due to Serious Tip-Over and Entrapment Hazards
Ameriwood recalls Mainstays chests of drawers that can tip over or get stuck, risking injury to children. These chests were sold with plastic drawer glides and a single decorative pull. Consumers should stop using unanchored units and contact Ameriwood for a free repair kit.
AmeriwoodSep 6, 2017 - Use cautionVehicle
RAM 1500 (2016) recall — Air Bags
Chrysler recalls 2016 RAM 1500 vehicles with potential air bag and seat belt failure during crashes if roll sensor faults occur. Owners must update ORC software to prevent injury.
ChryslerSep 5, 2017 - Use cautionVehicle
JEEP COMPASS (2017) recall — Power Train
Chrysler recalls certain 2017 Jeep Compass vehicles with 6-speed transmission due to potential left front halfshaft disengagement or breakage, which may cause loss of drive or rolling without parking brake.
ChryslerSep 5, 2017 - Stop using nowVehicle
CHEVROLET SPARK (2017) recall — Air Bags
GM recalls 2016-2017 Chevrolet Spark vehicles due to a risk of neck injury to unbelted children in the front seat during air bag deployment.
ChevroletSep 5, 2017 - Stop using nowMedical device
Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company recalls Irrisept OR, Finished Bottle Assembly 450 ml STEP 1
Smiths Medical recalls Irrisept OR 450ml bottles due to leaking containers that could expose users to infectious agents. Affected units include specific model and lot numbers.
Smiths MedicalSep 5, 2017 - Lower riskMedical device
Forte Automation Systems Inc recalls Patient Positioning System with KRC2 controller using software versions 2.3.1 2.3.10 Product Usage: The patient
Forte Automation Systems recalls patient positioning systems with specific software versions due to potential communication failures between the system and accuracy filter during patient procedures.
Forte Automation SystemsSep 5, 2017 - Lower riskMedical device
Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company recalls Portex 5ml Normal Saline (0.9%) Unit Dose¿¿¿¿ ¿
Smiths Medical recalls Portex 5ml Normal Saline (0.9%) Unit Dose containers due to leaking containers that could expose users to infectious agents. Affected units have model # UD9005 and lot number B515.
Smiths MedicalSep 5, 2017 - Lower riskMedical device
Aesculap Implant Systems LLC recalls ELAN 4 Blade: ELAN 4 1-RING PIN CUTTER D1.0 ELAN 4 1-RING NEURO CUTTER+ SOFT D1.5 ELAN 4 1-RING NEURO CUTTER+ SOFT D2.0
Aesculap recalls ELAN 4 blade accessories sold without required 510(k) clearance. These surgical tools may not meet safety standards. Consumers should contact Aesculap for details.
AesculapSep 5, 2017 - Lower riskDrug
Llorens Pharmaceutical Corp. recalls Urin D/S Tablets Methenamine 81.6 mg, Sodium Biphosphate 40.8 mg, Phenyl Salicylate 36.2 mg, Methylene Blue 10.8 mg,
Llorens Pharmaceutical recalls Urin D/S Tablets due to potential subpotent or superpotent tablets that may not work as intended. This could lead to ineffective treatment. Contact for details.
Llorens PharmaceuticalSep 5, 2017 - Lower riskDrug
Aidarex Pharmaceuticals LLC recalls ENALAPRIL MALEATE Tablets, USP, 5MG, 90-count bottles, Rx only, MFG: Wockhardt Ltd., India; Packaged By: Aidarex
Aidarex Pharmaceuticals recalls 5mg enalapril tablets (NDC 33261-0693-90) repackaged by Wockhardt Ltd. from India due to impurities. This recall affects specific lots manufactured in 2018.
AidarexSep 5, 2017
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