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- Lower riskMedical device
Polymer Technology Systems, Inc. recalls PTS Panels Lipid Panel test strip: IVD Lipid Panel Test Strips Ref Number: 1710 Product Usage: PTS Panels Lipid Panel
Polymer Technology Systems recalls Lipid Panel test strips with lot P901 that may display Q901 instead of P901 on analyzers, causing incorrect results.
Polymer Technology SystemsJun 7, 2019 - Use cautionMedical device
Philips North America, LLC recalls Philips HeartStart MRx devices in use with the M3539A AC Power Module: M3535A, M3536A, M3536M, M3536MC, M3536M2,
Philips recalls HeartStart MRx devices using M3539A AC Power Module models M3535A through M3536M9. The AC power module may fail at a higher rate, causing device power loss or shock delivery issues if battery is not properly installed.
PhilipsJun 7, 2019 - Lower riskMedical device
Burlington Medical, LLC recalls Frontal Apron with Quick Drop Velcro Closure (no elastic), Product Number 401, Part Numbers RE401*M Product Usage:
Burlington Medical recalls frontal aprons with quick drop velcro closure due to potential inadequate radiation protection, increasing cancer and infertility risks from scatter radiation exposure during medical procedures.
Burlington MedicalJun 7, 2019 - Lower riskDrug
PharMEDium Services, LLC recalls Hydromorphone HCl in 0.9% sodium chloride, 0.5mg per mL, 1 mL in 3mL BD Syringe, PharMEDium 913 N Davis Ave Cleveland,
PharMEDium recalls hydromorphone injection syringes containing sulfite due to incorrect formulation. Affected lots from June 2019 have sulfite, a potential allergen. Consumers should contact the manufacturer for details.
PharMEDiumJun 7, 2019 - Lower riskDrug
Akorn Inc recalls Myorisan (isotretinoin capsules, USP), 40 mg, packaged in cartons of 30 Capsules containing 3 x 10 Prescription Packs,
Akorn recalls Myorisan 40mg isotretinoin capsules due to label mix-up in packaging. The secondary carton incorrectly states 40mg instead of 30mg, while the primary carton is labeled correctly. This may cause confusion about dosage.
AkornJun 7, 2019 - Stop using nowFood
Townsend Farms Inc recalls Kirkland Signature Three Berry Blend product, frozen, package in a plastic bag. Net wt. 4 lbs. UPC 0 96619 10105 4. The
Kirkland Signature frozen three berry blend is recalled due to potential Hepatitis A contamination. Check your UPC and best-by dates immediately.
Kirkland SignatureJun 7, 2019 - Stop using nowFood
DILIP CERAMICS DBA SHIVAM DISTRIBUT recalls Parivar brand Dry Dates (Kharek) Net Wt.14 oz. (400 g) Product of India Batch No. 127/BHBI
Parivar Dry Dates (14 oz) from India batch 127/BHBI contain high sulfites. Consumers should stop using due to potential health risks from sulfite exposure.
ParivarJun 7, 2019 - Stop using nowFood
Bobbie Baby inc recalls Bobbie Milk-Based Powder Companion Formula Net Wt. 14.1 oz. (400g) 22 servings per container Serving Size 4 scoops.
Bobbie Baby recalls milk-based powder formula because it may not provide adequate nutrition for some infants. Check lot numbers and use-by dates.
Bobbie BabyJun 7, 2019 - Lower riskFood
The Kroger Co recalls PRIVATE SELECTION FROZEN TRIPLE BERRY MEDLEY, 16 oz
Kroger recalls Private Selection Frozen Triple Berry Medley (16 oz) due to possible Hepatitis A contamination. Consumers should check product dates and UPC codes for affected items.
KrogerJun 7, 2019 - Use cautionMeat & poultry
Table 87 Frozen, LLC Recalls Pork Pizza Products Produced Without Benefit of Inspection
USDA recalls 649 pounds of pork pizza products made without federal inspection. Consumers should not eat or dispose of recalled items.
Table 87 FrozenJun 6, 2019 - Use cautionVehicle
ACURA ILX (2019) recall — Power Train
Acura is recalling certain 2016-2019 ILX vehicles due to excessive grease causing driveshaft separation, which may lead to loss of drive or unintended movement in Park. Owners should contact Acura for free repairs.
AcuraJun 6, 2019 - Use cautionVehicle
INTERNATIONAL HV (2020) recall — Wheels
Navistar recalls 2020 International HV Severe Service Diesel Trucks due to potential wheel separation from axle spindle, increasing crash risk. Owners should have steer axle hubs inspected by dealers for lubrication issues.
NavistarJun 6, 2019 - Lower riskMedical device
DRG Instruments GmbH recalls DRG Salivary Progesterone HS ELISA- IVD for the determination of progesterone in human saliva REF: SLV-5911 in vitro
DRG recalls salivary progesterone test kits for potential low results in saliva samples. This in vitro diagnostic kit may produce inaccurate low readings for samples under 20 pg/ml.
DRGJun 6, 2019 - Lower riskMedical device
Skeletal Kinetics, Llc recalls OsteoVation, Inject Bone Filler Kits, 5cc (part number 390-2005, manufacturing lot number 1129957) - Product Usage: The
Skeletal Kinetics recalls OsteoVation 5cc bone filler kits (part 390-2005, lot 1129957) due to mixing instructions mismatching product labels. No injuries reported.
Skeletal KineticsJun 6, 2019 - Stop using nowMedical device
Siemens Medical Solutions USA, Inc recalls Siemens Artis zee floor -Interventional Fluoroscopic X-Ray System Model Number: 10094135
Siemens recalls Artis zee floor interventional fluoroscopy systems with specific model numbers due to potential screw failure that could cause severe injuries to patients and staff during procedures.
SiemensJun 6, 2019 - UnratedDrug
Teva Pharmaceuticals USA recalls LOSARTAN POTASSIUM 50 mg TABLET BULK 90 count bottles and 1000 count bottles, NDC 00591-3746-00
Teva Pharmaceuticals USA recalls Losartan Potassium 50mg tablets due to impurity detected in active ingredient. Affected lots may pose health risks. Consumers should check product details and contact Teva for guidance.
TevaJun 6, 2019 - Stop using nowConsumer product
Xtreme Outdoor Products Recalls Climbing Sticks Due to Fall Hazard and Risk of Serious Injury
Xtreme Outdoor Products recalls climbing sticks with a fall hazard due to bolt failure. Stop using and return for full refund or store credit.
Xtreme Outdoor ProductsJun 6, 2019 - Lower riskMedical device
GETINGE US SALES LLC recalls PulsioFlex Monitoring System, Part Number: 6882747, Model Number: PC400 3 R0. Usage: The PulsioFlex Monitoring System
GETINGE recalls PulsioFlex Monitoring System (model PC400 3 R0) with internal error message 'restart or service' that may cause incorrect readings. Affected units have specific serial numbers.
GETINGEJun 5, 2019 - Lower riskMedical device
Qiagen Sciences LLC recalls Filter-Tips, 1500 ul (1024 tips/kitbox), REF 997024- REF: 997024 IVD: Used with the QIAGEN QIAsymphony SP/AS
Qiagen recalls Filter-Tips (1500 ul) used with QIAsymphony SP/AS instruments due to leaking tips in some lots. Affected lots: 0605020019 and 0605020020. Stop using if leaking.
QiagenJun 5, 2019 - Stop using nowDrug
P & L Developments, LLC recalls Cetirizine Oral Solution 1 mg/mL, Up & Up, Children's allergy relief, Antihistamine, Dye Free, Grape Flavor, 4 FL. oz.
Target's Up & Up children's allergy relief cetirizine oral solution is recalled due to potential bacterial contamination. Check lot numbers and expiration dates.
Up & UpJun 5, 2019 - Lower riskDrug
Sun Pharmaceutical Industries, Inc. recalls Allergy Relief D, Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg, Extended Release Tablets, USP, 20-count box,
Sun Pharmaceutical recalls Allergy Relief D tablets due to potential impurities that could cause harm. Affected products include 20-count boxes with specific UPC and lot numbers. Consumers should contact CVS Pharmacy for details.
Sun PharmaceuticalJun 5, 2019 - Lower riskFood
Baumer Foods Inc recalls Soy Sauce, 10 FL OZ
Baumer Foods recalls 10 fl oz soy sauce (Lot 19087, 3/28/2021) because it was mislabeled as soy sauce but contains Worcestershire sauce, an undeclared allergen.
Baumer FoodsJun 5, 2019 - Lower riskFood
Whole Foods Market recalls Sun-dried tomato pesto, sold by weight in plastic deli containers PLU code beginning with 256009
Whole Foods Market recalls sun-dried tomato pesto (PLU 256009) due to failure to label major allergens: milk, walnuts, and pine nuts. Consumers should check labels and avoid if allergic.
Whole Foods MarketJun 5, 2019 - Stop using nowConsumer product
Apple Recalls Three-Prong Wall Plug Adapters Included in World Travel Adapter Kit Due to Risk of Electric Shock
Apple recalls three-prong wall plug adapters in World Travel Adapter Kits sold before Feb 2015 due to electric shock risk if adapters break. Consumers should stop using and get free replacements.
AppleJun 5, 2019 - Lower riskMedical device
Cardiac Science Corporation recalls Powerheart¿ G5 Automatic AED
Cardiac Science recalls Powerheart G5 AEDs with specific PCB serial numbers due to insufficient documentation for compliance. Affected units may not meet safety standards.
Cardiac ScienceJun 4, 2019 - Lower riskMedical device
Inlightened Partners LLC recalls inLight Medical LED Pads used with Polychromatic light technology system
inLight Medical LED Pads with v-shaped notch cord connectors may cause power shutdowns. Recalled due to improper assembly risk of interruption.
Inlightened PartnersJun 4, 2019 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Ultra-Drive Irrigation Tubing Assembly, Reference Number 423834 - Product Usage: Item used with the UltraDrive System
Zimmer Biomet recalls Ultra-Drive Irrigation Tubing Assembly (lot numbers listed) due to insufficient shelf life data supporting 10-year label. Consumers should check if their product has listed lot numbers and contact for details.
Zimmer BiometJun 4, 2019 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls SOMATOM go.Now, Model No. 11061618 with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1. Product Usage: This
Siemens recalls certain SOMATOM go.Now CT scanners with specific software versions due to potential scanning workflow interruptions and diagnostic delays. Affected units may require patient rescan if issues arise.
SiemensJun 4, 2019 - Lower riskFood
MOWI USA LLC recalls Marine Harvest USA, Contains Fish: Atlantic Salmon, Premium 35 lbs, Product must be cooked before consumption.
MOWI USA recalls Atlantic Salmon products for potential Listeria monocytogens contamination. Products must be cooked before consumption. Check lots # 0003541028, 0003541007, 0003540180, 0003540171.
MOWI USAJun 4, 2019 - Stop using nowFood
Simply Fresco LLC recalls Full Circle Market Garden Style Salsa, Mild, Net Wt 16 oz, in jars, 8 jars per case.
Simply Fresco LLC recalls Full Circle Market Garden Style Salsa, Mild (16 oz jars) due to potential foreign material up to 3 mm in diameter.
Full Circle MarketJun 4, 2019
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