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- Stop using nowMedical device
Seca recalls Seca 402/403 Baby Scale Cart, Ref # 4020000009/ REF # 4030000009
Seca recalls baby scale carts with serial numbers 6002142000002-6002142001101 due to risk of wheels detaching, which could cause tipping and serious injury to babies left unattended.
SecaJun 19, 2019 - Lower riskMedical device
Andover Healthcare Inc. recalls Sterile Co-Flex NL 3" - Product Usage: Single Use secondary wound dressing or compression wrap.
Andover Healthcare recalls Sterile Co-Flex NL 3" single-use wound dressings due to incomplete packaging seals that could compromise sterility.
Andover HealthcareJun 19, 2019 - Lower riskMedical device
Pharmaceutical Innovations, Inc. recalls ElectroMist product codes: 36-3310-25 - Product Usage: Electrode conductivity spray solution.
Pharmaceutical Innovations recalls ElectroMist electrode conductivity spray solution (product codes 36-3310-25) due to potential failure in antimicrobial effectiveness testing. Affected units include specific lot numbers from 2014-2018.
Pharmaceutical InnovationsJun 19, 2019 - UnratedDrug
RXQ Compounding LLC recalls GLUTATHIONE 200MG/ML (MDV) INJECTION SOLN, 30 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH
RXQ Compounding LLC recalls glutathione injections due to lack of sterility assurance. Affected products include 200mg/ml injection solutions sold in 30ml vials. No remedy specified in official notice.
RXQ CompoundingJun 19, 2019 - Stop using nowFood
UNFI General Corporate recalls WOODSTOCK ORGANIC GRILLED RED PEPPER, NET WT 10. OZ, packaged in a plastic packaged marked with UPC Code: 4256301714.
Woodstock Organic grills red peppers recalled due to Listeria monocytogenes contamination. Consumers should avoid using these products as they pose a risk of serious illness.
Woodstock OrganicJun 19, 2019 - Use cautionVehicle
FORD E-450 (2018) recall — Equipment
SVO Group recalls 2017-2018 Ford E-350/E-450 shuttle buses with ASA Electronics Voyager monitors that may reverse camera images, increasing crash risk. Free harness relay capacitor modules provided to fix.
SVO GroupJun 18, 2019 - Use cautionVehicle
ISUZU FTR (2020) recall — Steering
Isuzu recalls 2018-2020 FTR vehicles with loose steering jam nuts that increase turning radius, raising crash risk. Owners must get free replacement nuts and torque adjustments.
IsuzuJun 18, 2019 - Lower riskMedical device
CooperSurgical, Inc. recalls LEEP Precision Integrated System 120V & LEEP Precision Generator, Model Nos. LP-10-120 & LP-20-120
CooperSurgical recalls LEEP Precision Integrated System 120V and Generator models LP-10-120 and LP-20-120 due to potential failure of cut, coagulate, or blend functions when using the foot pedal.
CooperSurgicalJun 18, 2019 - Lower riskMedical device
Howmedica Osteonics Corp. recalls Serrato 9.5mm X 90mm Polyaxial Screw Catalog Number 482619590 Serrato 9.5mm X 100mm Polyaxial Screw Catalog Number
Howmedica Osteonics recalls two types of Serrato polyaxial screws (90mm and 100mm) that were manufactured with incorrect lengths. This could lead to improper joint fixation during surgery.
Howmedica OsteonicsJun 18, 2019 - UnratedMedical device
Ad-Tech Medical Instrument Corporation recalls LSB Style Anchor Bolt. Labeled with the following parts: 13mm anodized anchor bolt body with anchor bolt cap containing
Ad-Tech recalls LSB Style Anchor Bolts sold between March 2019 and May 2019 due to non-sterile parts distributed without proper sterilization instructions, posing infection risks in surgical procedures.
Ad-TechJun 18, 2019 - Lower riskMedical device
DeRoyal Industries Inc recalls DeRoyal THE RESOURCE GROUP, CRANI PACK, REF 89-9211.07 custom surgical pack
DeRoyal's CRANI PACK surgical packs (REF 89-9211.07) are recalled due to potential sterility compromise from defective blunt cannulas. Affected units include Lot 49888830.
DeRoyalJun 18, 2019 - Lower riskMedical device
Ad-Tech Medical Instrument Corporation recalls Dual-Sided Interhemispheric, Grid, Intraoperative, Strip, Wyler Subdural Electrodes
Ad-Tech Medical recalls dual-sided subdural electrodes sold through May 2019 due to MR environment safety risks. These devices are approved for use in MRI but not intended for that purpose.
Ad-Tech MedicalJun 18, 2019 - Lower riskMedical device
Epimed International, Inc. recalls Versa - Kath Mini Kit, with plastic L.O.R Syringe 12g X 12in (30.5 cm), 5 units, Sterile ED, REF 181-2112, RX, (01)
Epimed recalls Versa Kath Mini Kit with mislabeled catheter size. The kit includes a 21-gauge catheter but labels state 12-gauge. This affects medical use for epidural anesthesia.
EpimedJun 18, 2019 - UnratedDrug
Premier Pharmacy Labs Inc recalls Droperidol Injectable Sterile Solution, 0.625mg/mL, 1mL in a 3mL Sterile Single-Use Syringe, Rx only, Premier Pharmacy
Premier Pharmacy recalls Droperidol Injectable Sterile Solution due to potential contamination risks from inadequate sterilization processes. Affected products include specific lot numbers and sizes. Contact for details.
Premier PharmacyJun 18, 2019 - Stop using nowFood
Nature's Touch Frozen Foods (West) recalls Signature Select Avocado Chunks, 12 oz. (340 g) Stand-up pouch Re-sealable, Keep Frozen; UPC 2113009412 Ingredient:
Nature's Touch recalls frozen avocado chunks due to Listeria monocytogenes found in samples. Consumers should check UPC 2113009412 for affected items.
Nature's TouchJun 18, 2019 - UnratedFood
Mott's LLP recalls Penafiel Mineral Spring Water 600mL (20.3 FL OZ) and Penafiel Mineral Spring Water 1.5 L (50.7 FL OZ) packaged in clear
Mott's LLP recalls Penafiel Mineral Spring Water 600mL and 1.5L bottles due to elevated inorganic arsenic levels. Consumers should avoid using these products.
Mott'sJun 18, 2019 - Stop using nowConsumer product
Home Meridian Recalls Corner Curio Cabinets Due to Tip-Over and Entrapment Hazards; Sold Exclusively at Havertys (Recall Alert)
Copeland recalls corner curio cabinets (models 115-P021664/115-P021665) sold at Havertys due to tip-over and entrapment risks for children. Consumers must stop using and return for refund or credit.
CopelandJun 18, 2019 - Use cautionVehicle
FOREST RIVER BERKSHIRE (2018) recall — Equipment
Forest River recalls 2017-2018 Berkshire Coach Ultra UL1912/UL1913 motorhomes due to heater cable corrosion causing fire risk. Owners must contact Ford for free engine block heater cable repair.
Forest RiverJun 17, 2019 - Use cautionMedical device
Intuitive Surgical, Inc. recalls da Vinci Surgical System, IS 4000; Endoscope Controller, Model Number: 372601-16 (UDI: 00886874114193) is included in
Intuitive Surgical recalls da Vinci Xi Endoscope Controller Model 372601-16 due to improper calibration causing potential thermal tissue injury and overly bright images during surgery.
Intuitive SurgicalJun 17, 2019 - Lower riskMedical device
Datascope Corp. recalls CS100 Intra-Aortic Balloon Pump, English, 220V; 0998-00-3013-55 For cardiovascular use.
Datascope recalls CS100 Intra-Aortic Balloon Pumps with serial numbers 0998-00-3013-55 due to potential battery run time issues. Revised labeling and training are provided to address the risk.
DatascopeJun 17, 2019 - Lower riskMedical device
Ortho-Clinical Diagnostics recalls VITROS Chemistry Products GLU Slides-Product Code:1707801. IVD VITROS Chemistry Products GLU Slides quantitatively
Ortho-Clinical Diagnostics recalls VITROS Chemistry Glucose Slides (Product Code 1707801) due to potential for inaccurate glucose test results. Affected units were sold with specific lot numbers and expiration dates.
Ortho-Clinical DiagnosticsJun 17, 2019 - UnratedDrug
Bausch & Lomb recalls Lotemax (loteprednol etabonate ophthalmic gel 0.5%), Sterile, Rx Only, 5 g box, Bausch & Lomb, a division of Valeant
Bausch & Lomb recalls Lotemax (0.5% loteprednol etabonate ophthalmic gel) due to failed stability specifications. Affected lots expire 10/2019 or 11/2019. Contact for details.
Bausch & LombJun 17, 2019 - UnratedFood
Brand Castle LLC recalls Chocolate Mint Chip Cookie Mix, 27.1 oz glass jar, 6/case
Brand Castle recalls Chocolate Mint Chip Cookie Mix (27.1 oz glass jar, 6/case) due to potential E. coli contamination in flour. Consumers should check lot numbers and contact the company for details.
Brand CastleJun 17, 2019 - Lower riskFood
C & S Wholesale Grocers, Inc. recalls DANNON OIKOS TRIPLE ZERO GREEK VANILLA - 5.3OZ/4PK, UPC: 3663201953
DANNON OIKOS Triple Zero Greek Vanilla yogurt recalled due to temperature issues during shipping. Products sold at Target in NY June 2019 may be unsafe.
DANNONJun 17, 2019 - Lower riskFood
Mai Cuisine LLC recalls Spicy Shrimp Tempura Crunch Roll, Mai brand, packed in container with clear plastic lid,net wt. 9.1 oz., UPC 8 12824
Mai recalls Spicy Shrimp Tempura Crunch Roll (9.1 oz) due to undeclared egg allergen. Check UPC 8 12824 for affected items sold between June 15-17, 2019.
MaiJun 16, 2019 - Lower riskMeat & poultry
Table 87 Frozen, LLC Recalls Pork and Beef Pizza Products Produced without Benefit of Inspection
USDA recalls Table 87 frozen pizza products made without federal inspection. Consumers should not eat these pork and beef pizzas from June 3, 2017 to June 4, 2019.
Table 87Jun 14, 2019 - Use cautionMeat & poultry
Ruiz Foods Products Inc. Recalls Bacon Breakfast Wrap Products Due to Possible Foreign Matter Contamination
USDA FSIS recalls 246,514 pounds of frozen bacon breakfast wraps due to possible small rock contamination. Consumers urged to discard or return products.
Ruiz FoodsJun 14, 2019 - Use cautionVehicle
MERCEDES-BENZ AMG GT (2017) recall — Power Train
Mercedes-Benz USA is recalling 2016-2017 AMG GTS and GT vehicles due to potential driveshaft separation causing loss of drive and increased crash risk. Owners must contact MBUSA for free replacement of carbon-fiber driveshaft.
Mercedes-BenzJun 14, 2019 - Use cautionVehicle
GILLIG LOW FLOOR (2019) recall — Structure
Gillig recalls 2018-2019 Low Floor vehicles with certain glass roof hatches that may shatter due to temperature and vibration, risking glass fragments falling on passengers.
GilligJun 14, 2019 - Use cautionVehicle
PETERBILT 520 (2020) recall — Exterior Lighting
Paccar recalls certain 2020 Peterbilt 520 trucks with rear amber turn signals that may light up with brake lights, risking crashes. Owners must contact Paccar for free fix.
PaccarJun 14, 2019
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