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
34,894 found- Lower riskMedical device
Stryker Medical Division of Stryker Corporation recalls 6381 M-1 Cot Fastener, catalog no. 6381000000
Stryker recalls 6381 M-1 Cot Fasteners with missing safety warnings in manuals. Owners should check serial numbers 170740538-170740540 for affected units.
StrykerMar 9, 2018 - Lower riskMedical device
The Binding Site Group, Ltd. recalls Binding Site Optilite Beta-2-Microglobulin Urine Kit, Ref LK043.L.OPT.A, IVD. The firm name on the label is The Binding
The Binding Site Group recalls their Optilite Beta-2-Microglobulin Urine Kit (Ref LK043.L.OPT.A) due to inaccurate test results. This IVD kit may not meet the claimed antigen excess protection level of 760mg/L, potentially leading to incorrect diagnosis of rheumatoid arthritis or kidney disease.
The BindingMar 9, 2018 - UnratedDrug
Akorn, Inc. recalls Triamcinolone Acetonide Lotion, USP 0.1%, 60 mL bottle, Rx Only, Marketed by: VersaPharm Incorporated, Marietta, GA
Akorn recalls 60mL Triamcinolone Acetonide Lotion (Rx only) due to high impurity levels. This medication may contain unsafe substances that could cause health risks. Consumers should contact the manufacturer for details.
AkornMar 9, 2018 - Lower riskDrug
Alva-Amco Pharmacal Companies., Inc. recalls Psoriasin Daytime Relief Cream with Vitamin D & Oatmeal, (Coal Tar 1.25%), packagedin 57 g plastic tubes, Distributed
Alva-Amco recalls Psoriasin Daytime Relief Cream with Vitamin D & Oatmeal due to coal tar content failing label claims. Product may not provide intended relief after 24 months.
Alva-AmcoMar 9, 2018 - Lower riskFood
Nestle Dreyers Ice Cream Company recalls Dreyer's Slow Churned Vanilla Bean Ice Cream; 1.5 qt, (48-fl oz.); Lid is for Dreyer's Slow Churned Butter Pecan Ice
Nestle Dreyer's recalls 48-fl oz. vanilla bean ice cream with butter pecan lid. Wrong lid may cause confusion and incorrect use. Stop using and check for matching lid.
Dreyer'sMar 9, 2018 - Stop using nowFood
Oregon Food Bank recalls Chia Seeds packaged in poly film bags as both a twist type closure and a re-sealable pouch, net wt. 1 lb.
Oregon Food Bank recalls 1 lb chia seeds packaged in poly film bags with twist closure and re-sealable pouch due to rodent contamination. Consumers should stop using these products immediately.
Oregon Food BankMar 9, 2018 - Lower riskFood
Avalon Packaging recalls NXTGEN Botanicals, Maeng Da Kratom, Dietary Supplement, 70 Capsules, Made in the U.S.A
Avalon Packaging recalls 70-capsule Kratom supplements due to potential Salmonella contamination. Consumers should check lot numbers for affected products.
Avalon PackagingMar 9, 2018 - Stop using nowFood
Pdx Aromatics recalls RED Kratom CAPSULES, sold under brand names Kraken Kratom, Phytoextractum, and Soul Speciosa. The capsules are packaged
Pdx Aromatics recalls Red Kratom capsules from brands like Kraken and Phytoextractum due to potential Salmonella contamination. Check lot codes.
Pdx AromaticsMar 9, 2018 - Use cautionVehicle
HONDA CRF1000A (2018) recall — Structure
Honda recalls 2016-2018 Africa Twin motorcycles with specific centerstand kits due to risk of detachment causing crashes or falls. Affected owners should contact Honda for free replacement.
HondaMar 8, 2018 - Lower riskMedical device
Southern Implants, (Pty.) Ltd. recalls SOUTHERN IMPLANTS REF IBR12d-13, Implant, Ext. Hex, tapered 12o Co-Axis(TM) intended for surgical placement in the
Southern Implants recalls specific dental implants due to incorrect labeling on inner labels. This may cause confusion in surgical use. Affected units have lot code 251J00d2.
Southern ImplantsMar 8, 2018 - UnratedDrug
Jimmy Weber recalls Red Zone Xtreme 3000 Capsules, Dietary Supplement Product, 1 count blister pack, UPC 8 91656 00200 9, Exp Date
Jimmy Weber recalls Red Zone Xtreme 3000 Capsules dietary supplements due to undeclared Tadalafil, an FDA-approved erectile dysfunction drug, found in the product.
Jimmy WeberMar 8, 2018 - UnratedDrug
Bracco Diagnostics Inc. recalls E-Z-Paste Barium Sulfate Esophageal Cream (60% w/w), 454 g tube, Rx only, Manufactured by E-Z-EM Canada Inc. for E-Z-EM
Bracco Diagnostics recalls E-Z-Paste Barium Sulf: 454g tube with failed stability test for methylparaben. No remedy stated in official notice.
Bracco DiagnosticsMar 8, 2018 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Clocortolone Pivalate Cream, 0.1%, 90-gram tube, Rx only, Distributed by: Dr. Reddy's Laboratories, Inc. Princeton, NJ
Dr. Reddy's recalls 0.1% Clocortolone Pivalate Cream tubes due to stability testing failures. This cream may not be effective or safe after expiration.
Dr. Reddy'sMar 8, 2018 - Stop using nowFood
ADM Agri Industries recalls Provim ESP Vita Wheat Gluten, Product code 6303, 50 lb bag
ADM recalls Provim ESP Vita Wheat Gluten (50 lb bags) due to Listeria monocytogenes contamination. Consumers should avoid using these products to prevent potential foodborne illness.
ADM Agri IndustriesMar 8, 2018 - Stop using nowConsumer product
Golden State Warriors Menorahs Recalled by BDA Due to Fire and Burn Hazards (Recall Alert)
Recalled Golden State Warriors Menorahs from Jewish Heritage Night promotions pose fire and burn risks due to melting glue causing candleholders to fall off. Consumers should stop using and dispose of them.
Golden State WarriorsMar 8, 2018 - Use cautionVehicle
COACHMEN FREELANDER (2017) recall — Visibility
Forest River recalls 2017 Freelander vehicles with driver side power window switch that may leak liquid causing corrosion and fire risk. Owners must contact customer service for free replacement.
Forest RiverMar 7, 2018 - Use cautionMedical device
Autochair recalls Product: Milford Smartbase Model # 9934105 Pride SmartBase Pride product codes: LSMPLCG A & LSMPLCG B
Autochair's Milford Smartbase model 9934105 Pride SmartBase (product codes LSMPLCG A/B) may fold inward when lifting users, causing drops. Affected units include all lots sold.
AutochairMar 7, 2018 - Lower riskMedical device
Smith & Nephew, Inc. recalls D-RAD Self-Tapping Locking Screw intended for the fixation of fractures involving the distal radius. smith&nephew D-RAD
Smith & Neph: D-RAD Self-Tapping Locking Screws (Lot 17GM04522) may have over-tolerance threads causing improper fracture fixation. Affected patients should contact manufacturer for details.
Smith & NephewMar 7, 2018 - Lower riskMedical device
SPS Sterilization, Inc recalls Edwards Lifesciences Avid Dual Stage Venous Drainage Cannula, 29/37F (9.6/12.3MM) X 37CM (14.5"), resterilized.
Edwards Lifesciences recalls resterilized Avid Dual Stage Venous Drainage Cannulas due to expiration date exceeding validated shelf life. Affected units have specific codes and serial numbers.
Edwards LifesciencesMar 7, 2018 - Use cautionMedical device
Intuitive Surgical, Inc. recalls da Vinci X Surgical System, Model IS4200. Product Usage: The Intuitive Surgical Endoscopic Instrument Control System
Intuitive Surgical recalls da Vinci X Surgical System Model IS4200 with defective Arm Controller Joint (ACJ) boards that may fail, potentially causing system malfunctions during surgery.
Intuitive SurgicalMar 7, 2018 - UnratedMedical device
Ethicon, Inc. recalls Evicel Accessory Device - 45 cm Flexible Tip (SET OF 3), Product Code EVT45. Accessory Tips for use only with EVICEL
Ethicon recalls 45cm flexible tip accessory set (EVT45) distributed in US. Products labeled for outside US may have been sold here. No remedy specified in recall notice.
EthiconMar 7, 2018 - Lower riskDrug
American Pharmaceutical Ingredients LLC recalls Oxytocin USP, powder, 1g-bottle, API American Pharmaceutical Ingredients, NDC 58597-7042-3
American Pharmaceutical Ingredients LLC recalls Oxytocin USP powder (1g bottles) due to stability data not supporting listed expiry dates. No remedy specified in official notice.
American Pharmaceutical IngredientsMar 7, 2018 - Lower riskDrug
Apollo Care recalls Vancomycin 1.25g added to 250 mL of 0.9% Sodium Chloride IV bag, Rx only, APOLLOcare, 3801 Mojave Ct., Suite 101,
Apollo Care recalls Vancomycin 1.25g IV bags due to stability concerns beyond 90 days from use date. This affects certain lots manufactured in 2018. No immediate action needed but check expiration dates.
Apollo CareMar 7, 2018 - Lower riskFood
Oregon Wild Berries, Inc. recalls Mushroom Condensed Soup, brand Chef Edwin's, packaged in glass pint Kerr jars, Net wt. 14 oz. UPC 7 00424 66845 8. The
Oregon Wild Berries, Inc. recalls Chef Edwin's Mushroom Condensed Soup in glass pint Kerr jars due to under-processing. Consumers should check labels for UPC 7 00424 66845 8 and use by date OCT 2019.
Chef Edwin'sMar 7, 2018 - Use cautionConsumer product
Topson Downs Recalls Cat & Jack Girls' Star Studded Jeans Due to Laceration Hazard; Sold Exclusively at Target
Topson Downs recalls Cat & Jack Girls' Star Studded Skinny Jeans due to metal stars that can detach and cause lacerations. Return to Target for full refund.
Cat & JackMar 7, 2018 - Stop using nowConsumer product
Husqvarna Motorcycles Recalls Closed Course Competition Motorcycles Due to Crash Hazard (Recall Alert)
Recall of 2016-2018 Husqvarna FS 450 closed course motorcycles due to risk of brake failure causing crashes. Affected models have specific VIN codes and colors.
HusqvarnaMar 7, 2018 - Use cautionConsumer product
First Aid Research Recalls Maximum Strength Bacitraycin Plus Ointment With Lidocaine Due to Failure to Meet Child Resistant Closure Requirement
First Aid Research recalls Maximum Strength Bacitraycin Plus Ointment with Lidocaine due to non-child-resistant packaging. This poses a poisoning risk to young children if ingested or applied to skin.
First Aid ResearchMar 7, 2018 - Lower riskMedical device
Integra LifeSciences Corp. recalls Manuka Honey Wound Gel Catalogue No: 716597 Product Usage: Helps maintain a moist wound environment which has shown to
Integra LifeSciences recalls Manuka Honey Wound Gel (Catalogue No: 716:597) due to an incorrect gel part number in manufacturing records. This may affect wound healing for minor injuries.
Integra LifeSciencesMar 6, 2018 - Lower riskFood
Piggie Park Enterprises Inc recalls Maurice's Honey Southern Gold BBQ Sauce; Net Wt. 18 oz. bottles; UPC Code 0 7561654332 6 and Carolina Gold Honey Sauce;
Piggie Park Enterprises recalls Maurice's Honey Southern Gold BBQ Sauce (18 oz) and Carolina Gold Honey Sauce due to undeclared soy and wheat ingredients. Consumers should check UPC codes 075616543326 and 075616543838 for affected products.
Maurice's HoneyMar 6, 2018 - Lower riskFood
Josie's Homestyle Pralines Etc. Inc. recalls Josie's Homestyle #1 Pralines Net Wt. 2 oz (57 g) bag INGREDIENTS: Sugar, Cream, Pecans, Butter, Vanilla, if (Rum) Rum
Josie's Homestyle recalls pralines bags due to mislabeled cream and butter ingredients, potentially causing confusion about actual contents.
Josie's HomestyleMar 6, 2018
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