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
34,959 found- Use cautionVehicle
FOREST RIVER CHEROKEE (2020) recall — Equipment
Forest River is recalling 2020 Cherokee Alpha Wolf travel trailers due to a wiring issue that could cause fire. Owners should contact customer service for free repairs.
Forest RiverJan 11, 2019 - Lower riskMedical device
Organon Teknika Inc recalls Vitek 2 reagent cards: a) GN ID, REF 21341, b) GP ID, REF 21342, c) ANC ID, REF 21347, d) AST-GNOR, REF 22000, e)
Organon Teknika recalls Vitek 2 reagent cards with potential for false antibiotic resistance results, false negative ESBL tests, and false positive urea reactions. Affected lots listed in the recall notice.
Organon TeknikaJan 11, 2019 - Use cautionMedical device
AAP Implantate Ag recalls aap Implante AG, Lambotte chisel, 20 mm, REF IU 3000-20 Product Usage: Surgical instruments are intended to aid in the
AAP Implantate Ag recalls Lambotte chisels (20mm, REF IU 3000-20) due to potential breakage at welded parts during surgical use. Affected units include specific lot numbers.
AAP Implantate AgJan 11, 2019 - Lower riskMedical device
Lin-Zhi International Inc recalls Ethyl Alcohol Enzymatic Assay, (a) REF 0220 (small test kit), (b) REF 0221 (large test kit) Product Usage: Detergent
Lin-Zhi International recalls two ethyl alcohol test kits that may degrade faster when detergent residue is present, reducing shelf life. Consumers should check lot codes and contact the company for details.
Lin-ZhiJan 11, 2019 - Lower riskDrug
Oxalis Labs recalls Clobetasol Propionate Topical Solution USP, 0.05% w/w, 50 mL bottle, Manufactured for: Macleods Pharma USA, Inc.
Oxalis Labs recalls 0.05% Clobetasol Propionate Topical Solution bottles due to leakage complaints. Affected units have specific lot numbers and expiration dates. Consumers should check their product details.
Oxalis LabsJan 11, 2019 - Stop using nowFood
McCormick & Company, Inc. - Flavor Manufacturing Center recalls El Guapo Pasilla-Ancho Chile Pods 2oz, 7.5oz, 11oz
El Guapo Pasilla-Ancho Chile Pods are recalled due to unlabeled peanut allergen. Check UPCs and best-by dates for affected lots.
El GuapoJan 11, 2019 - Stop using nowFood
Nutrafuels, Inc. recalls CTFO Pain Relief Oral Spray with pure CBD Hemp Oil isolate Dietary Supplement, 1oz/30ml.
Nutrafuels recalls CTFO Pain Relief Oral Spray with microbial contamination in specific lots. Consumers should stop using affected products to avoid potential health risks.
NutrafuelsJan 11, 2019 - Use cautionVehicle
JAYCO REDHAWK (2019) recall — Electrical System
Jayco is recalling 2019-2020 Redhawk SE motorhomes with a seatbelt warning light that doesn't illuminate for 5 seconds after ignition. This could cause drivers to forget seatbelts in crashes.
JaycoJan 10, 2019 - Use cautionVehicle
BMW K 1600 GTL (2019) recall — Power Train
BMW recalls 2019 K 1600 GTL motorcycles with potential transmission issues causing rear wheel lockup and crash risk. Owners must contact BMW for free replacement of shift forks and gear components.
BMWJan 10, 2019 - Lower riskMedical device
Arrow International Inc recalls Arrow¿ Two-Lumen Central Venous Catheterization Set with Blue FlexTip¿ Catheter Product Code: CD-10802 GTN:
Arrow recalls two-lumen central venous catheter sets with blue flextip catheters due to incorrect priming volume labeling on the lidstock. This may cause errors in medical procedures.
ArrowJan 10, 2019 - Lower riskMedical device
Bio-Rad Laboratories, Inc recalls EVOLIS Microplate System (Catalog no. 89700) with TimeLiner Data Management Software, (Catalog no. 90471A.
Bio-Rad recalls EVOLIS Microplate System with TimeLiner software due to potential for incorrect lab results. Affected units may need correction to prevent errors in laboratory testing.
Bio-RadJan 10, 2019 - Lower riskMedical device
Ottobock Orthopedic Industrie recalls 21Y15 MagValve Product Usage: The PushValves/ MagValves is intended exclusively for the prosthetic fitting of lower
Ottobock recalls 21Y15 MagValves for lower limb prosthetics sold 2017-2018 due to valve diameter smaller than spec. Affected users should check product details.
OttobockJan 10, 2019 - Lower riskMedical device
PerkinElmer Life and Analytical Sciences, Wallac, OY recalls AutoDELFIA¿ hCG Kit, In Vitro Diagnostic for the determination of human gonadotropin (hCG) Product Code: B007-112 -
PerkinElmer recalls AutoDELFIA hCG Kit (Product Code B007-112) due to potential 15-20% lower hCG analyte concentrations at low measurement ranges. Affected kits have specific lot numbers.
PerkinEl:merJan 10, 2019 - Lower riskDrug
McGuff Compounding Pharmacy Services, Inc. recalls Lipoic Acid Injection (aka Alpha Lipoic Acid or Thioctic Acid), 1,200 mg/30 mL (40 mg/mL) Sterile 30 mL Multiple Dose
McGuff Compounding Pharmacy recalls Lipoic Acid Injection vials with visible particulate matter. This may cause injection site reactions. Check your vial lot number for affected units.
McGuffJan 10, 2019 - Lower riskDrug
MAJOR PHARMACEUTICALS recalls Losartan Potassium Tablets, USP. 50 mg. NDC# 0904-6390-61. Rx only. 100 count Unit Dose Cartons. Manufactured by Major
Major Pharmaceuticals recalls 50mg Losartan Potassium Tablets (NDC 0904-6390-61) due to FDA-confirmed NMBA impurity exceeding safe levels. Rx-only medication sold in 100-count unit dose cartons.
Major PharmaceuticalsJan 10, 2019 - Use cautionMeat & poultry
J. H. Routh Packing Co. Recalls Pork Sausage Products due to Possible Foreign Matter Contamination
USDA recalls 1,719 pounds of Daisyfield pork sausage products from Jan. 1-4, 2019, due to possible rubber contamination. Consumers are urged not to consume these products.
DaisyfieldJan 9, 2019 - Use cautionMedical device
Implant Direct Sybron Manufacturing LLC recalls SwishPlus Implant 5.7mmD x 8mmL, SBM 6.5mmD Platform, Part Number 925708
Implant Direct recalls SwishPlus Implant 5.7mmD x 8mmL due to incorrect color coding on vials and caps, potentially causing surgical errors. Affected units have specific part numbers and were not distributed in the US.
Implant DirectJan 9, 2019 - Lower riskMedical device
Karl Storz Endoscopy recalls Insufflation tubing to be used with varies insufflator units. REF 031200-10; REF 031322-10; REF 031532-10; REF 031622-10
Karl Storz recalls insufflation tubing with higher ethylene oxide residues than safe levels. Affected units include specific model/lot numbers. Consumers should check their tubing for the listed serial numbers.
Karl StorzJan 9, 2019 - Lower riskMedical device
NEUSOFT MEDICAL SYSTEMS IMP & EX recalls NeuViz 128 Multi-slice CT Scanner System with software version 1.0.8.5010O+P04 Vi .0.8.521 9+PO1 Multi-Slice CT Scanner
NeuViz 128 Multi-slice CT Scanner with software version 1.0.8.5010O+P04 may produce incorrect scan images if used for scans longer than 500mm. Affected units have series numbers N1281180242E, N1281170231E, N1281180248E.
NeusoftJan 9, 2019 - Lower riskMedical device
ConvaTec, Inc recalls Nelaton Urinary Catheter, disposable, sterile, 100 eaches per sales unit. Labeled as: CH16/40CM and CH14/40CM Product
ConvaTec recalls Nelaton urinary catheters with potential sterile packaging breach. These disposable catheters may risk infection if not properly sealed. Consumers should check labels for CH16/40CM or CH14/40CM models.
ConvaTecJan 9, 2019 - Use cautionMedical device
Philips North America, LLC recalls PageWriter TC70, Product 860315, Software revisions up to and including A.07.05.22 used to evaluate the
Philips recalls PageWriter TC70 cardiograph devices with software revisions up to A.07.05.22 that may overheat, melt, or ignite due to end-of-life batteries. This poses a risk of injury to patients or nearby users. Affected units include specific model numbers and software versions.
PhilipsJan 9, 2019 - Lower riskDrug
Lupin Pharmaceuticals Inc. recalls Cephalexin for Oral Suspension USP 250mg/5 mL, Rx Only Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore,
Lupin Pharmaceuticals recalls Cephalexin 250mg/5mL oral suspension (Rx only) due to possible sucrose contamination in packaging. Affected lots manufactured in Baltimore, Maryland, with NDC 68180-441-01.
LupinJan 9, 2019 - Use cautionVehicle
WINNEBAGO FUSE (2018) recall — Wheels
Winnebago is recalling 2018-2019 Fuse motorhomes with aluminum wheel feature code 63W due to potential wheel detachment. Owners must contact Winnebago for free replacement of wheel studs.
WinnebagoJan 8, 2019 - Use cautionVehicle
TOYOTA CAMRY (2019) recall — Air Bags
Toyota recalls 2019 Camry vehicles with improperly calibrated air bags that may not deploy in crashes, risking passenger injury. Owners must contact Toyota for free recalibration.
ToyotaJan 8, 2019 - Stop using nowVehicle
HONDA CR-V (2019) recall — Fuel System, Gasoline
Honda recalls certain 2019 CR-V vehicles due to a failed fuel tank weld that may cause leaks and increase fire risk. Dealers will replace the tank free of charge.
HondaJan 8, 2019 - Use cautionVehicle
THOR MOTOR COACH OMNI (2020) recall — Equipment
Thor Motor Coach is recalling certain 2019-2020 Omni motorhomes due to potential battery tray detachment causing vehicle stalling and crash risk. Owners should contact TMC for free repair.
Thor Motor CoachJan 8, 2019 - Stop using nowMedical device
GETINGE US SALES LLC recalls Maquet XS Flat Screen Monitor Holder, XS32 SPE, Configuration Part Number ARD22201040A Product Usage: This product is
GETINGE recalls Maquet XS Flat Screen Monitor Holders with serial numbers 500009-500014 due to potential electric shock risk from improper grounding. Affected units may cause mild to severe electric shock when used with 100-220V power.
GETINGEJan 8, 2019 - Stop using nowDrug
Happy Together, Inc. recalls 5K Premium Enhancement capsule, 5000 mg, 1 count blister card, box of 30, Happy Together Inc., Boynton, FL UPC
FDA recalls Happy Together's 5K Premium Enhancement capsules due to undeclared sildenafil and tadalafil. Check your bottle if bought online.
Happy TogetherJan 8, 2019 - Stop using nowFood
Winter Gardens Quality Foods, Inc. recalls Chips & Chocolate, A layered dessert with chocolate mousse layer on the bottom, with a white whipped topping layer on
Winter Gardens recalls 5-lb Chips & Chocolate dessert products potentially contaminated with Salmonella. Consumers should avoid these items due to food safety risks.
Winter GardensJan 8, 2019 - Stop using nowVehicle
FOREST RIVER ROCKPORT (2019) recall — Electrical System
Forest River recalls certain 2019 Rockport work trucks due to improperly wired trailer brake controllers that may fail to activate, increasing crash risk.
Forest RiverJan 7, 2019
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