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 riskDrug
ImprimisRx NJ recalls Timolol- Dorzolamide- Latanoprost P-F (0.5/2.0/0.005%) ophthalmic drops, packaged in 5mL bottles, Rx only, ImprimisRx
ImprimisRx recalls specific ophthalmic drops due to subpotent drug content. This may affect prescription eye drops with lot numbers 03132019@2 and 05102019@2. Contact for details.
ImprimisRxJul 17, 2019 - Stop using nowConsumer product
Bodum Recalls Toasters Due to Shock Hazard
Bodum recalls Bistro toasters due to shock hazard. Stop using immediately and return for a full refund.
BodumJul 17, 2019 - Use cautionVehicle
TOYOTA SIENNA (2020) recall — Steering
Braun recalls certain 2017-2020 Toyota Sienna vehicles with potentially fractured steering shaft extensions that could cause loss of steering and crash risk. Owners must contact Braun for free replacement.
BraunJul 16, 2019 - UnratedMedical device
TeDan Surgical Innovations LLC recalls Fukushima suction tubes; Fukushima Malleable Tapered Suction, 3 FR, 145 MM; REF: TK-1110 - Product Usage: TSI Fukushima
TeDan Surgical Innovations recalls Fukushima Malleable Tapered Suction tubes (Lot 0619) due to incorrect raw materials used in production. These reusable surgical instruments are used in hospitals to remove debris and blood during procedures.
TeDan Surgical InnovationsJul 16, 2019 - Lower riskMedical device
Luminex Molecular Diagnostics recalls xTAG Respiratory Viral Panel (RVP): Box Label: xTAG RVP (Respiratory Viral Panel). Catalogue Number:I019C0111 in vitro
Luminex recalls xTAG Respiratory Viral Panel (RVP) with catalogue number I019C0111 due to potential false negative results for Influenza A (H3) and RSV A. This may lead to missed diagnoses but does not affect other virus detection.
LuminexJul 16, 2019 - Lower riskMedical device
Roche Diagnostics Operations, Inc. recalls Roche Elecsys Anti-CCP Immunoassay Catalog # 05031656160
Roche recalls specific lots of Elecsys Anti-CCP assay kits for performance issues with cobas e 411, e 170, and other analyzers. Affected lots distributed from Feb 2019 to July 2019.
RocheJul 16, 2019 - Use cautionMedical device
Canadian Hospital Specialties recalls MED-RX POLYURETHANE FEEDING TUBES: a) 5Fr X 16" (40cm), REF 54-1650R b) 6.5Fr X16" (40cm), REF 54-1665R c) 5Fr X 24"
Canadian Hospital Specialties recalls MED-RX polyurethane feeding tubes with a connector that may detach, posing a risk of disconnection during use. Affected models include 5Fr X 16" (40cm) and others with specific reference numbers and lot numbers.
Canadian Hospital SpecialtiesJul 16, 2019 - UnratedMedical device
Philips North America, LLC recalls HeartStart MRx Monitor/Defibrillator Model # M3535A - Product Usage: The HeartStart MRx is a lightweight, portable
Philips recalls HeartStart MRx Monitor/Defibrillator Model M3535A due to potential non-conforming devices that may not have been corrected in prior actions. Affected units include specific lot numbers.
PhilipsJul 16, 2019 - Use cautionMedical device
Philips North America, LLC recalls Philips Azurion systems with software version R1.2 -Interventional Fluoroscopic X-ray system as follows: Azurion 3 M12,
Philips recalls Azurion 3 M12, M15, 7 B12, B20, M12, M20 models with R1.2 software due to potential 7-minute cold restart delays after 50 days of mains power use, risking treatment delays.
PhilipsJul 16, 2019 - UnratedDrug
Bionpharma Inc. recalls Clobazam Oral Suspension, 2.5 mg/mL, 120 mL bottle, Rx only, Distributed by: Bionpharma Inc., 600 Alexander Road,
Bionpharma recalls Clobazam oral suspension (2.5 mg/mL, 120mL) due to microbial contamination. This may cause health risks if used. Affected lots: 18246 (exp 09/2020).
BionpharmaJul 16, 2019 - Lower riskDrug
Deva Holding AS - Cerkezkoy Subesi recalls Temozolomide Capsules, 180 mg, packaged in a) 5-count bottle (NDC 67877-541-07), b) 14-count bottle (NDC 67877-541-14),
Deva Holding recalls Temozolomide 180mg capsules due to possible cross contamination with beta-lactam products during manufacturing. Affected lots expire through 2021.
Deva HoldingJul 16, 2019 - Lower riskFood
FRUNUT GLOBAL COMMODITIES LLC recalls Fruits Du Sud Golden Raisins, Golden Seedless Raisins, - Grade Medium Choice - Crop 2018 Net Weight 30LB (13.6KG),
Fruits Du Sud Golden and Seedless Raisins from Crop 2018 with undeclared sulfites recalled. Consumers should check labels for lot number FDS T690/18.
Fruits Du SudJul 16, 2019 - Lower riskFood
Jelly Belly recalls Jelly Belly Licorice Bridge Mix. Net Wt. 9 oz. (85g); 12 individual 3 oz. bags per caddy UPC: 071567981675 Manufactured
Jelly Belly recalls 9oz Licorice Bridge Mix due to gluten contamination in products labeled gluten-free. Check UPC 071567981675 for affected items.
Jelly BellyJul 16, 2019 - Lower riskFood
The Crystal Spoon Corp. recalls Top Chef Meals Grilled Bison Burger best used by date between 5/4/19-6/30/19 Unit Size: 6 and 8 oz sizes Container
Top Chef Meals Grilled Bison Burger (6-8 oz) recalled due to potential E. coli contamination. Best used by dates May 4-30, 2019. Consumers should check dates and contact for details.
The Crystal Spoon Corp.Jul 16, 2019 - Stop using nowFood
Diversified Foods and Seasonings LLC recalls Macaroni and Cheese packaged in 4 lb plastic bags, 12 bags per case, frozen
Diversified Foods recalls frozen macaroni and cheese in 4 lb bags due to plastic foreign material posing a choking risk.
Diversified FoodsJul 16, 2019 - Use cautionConsumer product
Wintergreen Essential Oil Recalled by Epic Business Services Due to Failure to Meet Child Resistant Closure Requirement; Risk of Poisoning (Recall Alert)
Majestic Pure Wintergreen essential oil is recalled due to non-child-resistant packaging. Young children could ingest it and be poisoned. Consumers should store safely and get a free child-resistant dropper replacement.
Majestic PureJul 16, 2019 - Use cautionConsumer product
VIVO Recalls Speaker Wall Mounts Due to Fall and Injury Hazards
VIVO recalls MOUNT-PLAY5 speaker wall mounts due to risk of speakers falling and causing injury to bystanders. Consumers must remove speakers and contact VIVO for free repair, replacement, or refund.
VIVOJul 16, 2019 - Stop using nowConsumer product
K2 Sports Recalls Inline Skates Due to Fall Hazard
K2 Sports recalls VO2 S inline skates due to risk of wheel separation causing falls. Affected models include VO2 S 90 PRO M, 90 PRO W, 100 PRO M, 100 X PRO W, and 100 BOA. Return for free repair.
K2 SportsJul 16, 2019 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls Dimension¿ Ferritin (FERR) Flex¿ reagent cartridge DM FERR Product Usage: The FERR Flex reagent cartridge is intended
Siemens Healthcare recalls Dimension Ferritin (FERR) Flex reagent cartridges with lot EA922: Negative bias may cause inaccurate ferritin measurements, affecting iron metabolism disease diagnosis.
Siemens HealthcareJul 15, 2019 - UnratedMedical device
Centurion Medical Products Corporation recalls PORT ACCESS INFUSION KIT - 1" NEEDLE Product Code: DYNDC2817
Centurion Medical recalls Port Access Infusion Kit 1" needles due to supplier-initiated recall of GRIPPER Needles. Affected units include Product Code DYNDC2817 with specific lot numbers.
Centurion MedicalJul 15, 2019 - Lower riskDrug
Unipharma, Llc. recalls DrKids Children's Allergy Relief Diphenhydramine HCl 12.5 mg/5 mL Antihistamine, Mixed berry Flavor, 20 Pre-measured
Unipharma recalls DrKids Children's Allergy Relief Diphenhydramine HCl 12.5 mg/5 mL antihistamine due to potential contamination with bacteria B. cepacia. This precautionary recall affects 20-pre-measured vials manufactured in the USA.
UnipharmaJul 15, 2019 - Lower riskDrug
La Fresh Group, Inc. recalls LA FRESH travel lite Sunnyside Lotion Wipe silky, non-greasy formula smooth, soft & moisturizing featuring titanium
La Fresh recalls Sunnyside Lotion Wipe due to potential sunscreen mislabeling without FDA approval. Check product lot numbers starting with 453091 for affected items.
La FreshJul 15, 2019 - Use cautionFood
Pita Pal Foods LP recalls PitaPal Mezza Sundried Tomato Hummus 11 oz. UPC 851351007336 packaged in Plastic tub with clear lid with green rim.
PitaPal Mezza Sundried Tomato Hummus (11 oz) with UPC 851351007336 may contain Listeria monocytogenes. Consumers should check packaging for recall details.
Pita Pal FoodsJul 15, 2019 - Use cautionMeat & poultry
Fieldsource Food Systems, Inc. Recalls Beef and Poultry Products Due to Misbranding and Undeclared Allergens
USDA recalls 12,953 pounds of Fieldsource marinated beef and chicken cubes due to undeclared wheat allergen. Products may cause allergic reactions; consumers should discard or return to store.
FieldsourceJul 14, 2019 - Lower riskMeat & poultry
Ada Valley Gourmet Foods, Inc. Recalls Beef Products Due to Possible Foreign Matter Contamination
Ada Valley Gourmet Foods recalls 3,490 pounds of raw ground beef meatloaf products that may contain broken metal bits. Consumers should check labels for lot code 17034 and packaging date 05-20-19.
Ada Valley MeatsJul 13, 2019 - Use cautionMedical device
Dexcom Inc recalls Dexcom Receiver, REF: MT22719, (Black, Pin, Blue), Rx Only, containing software version SW10617 and revision 4.0.1.048
Dexcom recalls G5 Mobile Receivers with specific software versions that may not display glucose readings or alerts properly. Affected units could miss critical diabetes management information.
DexcomJul 12, 2019 - Lower riskMedical device
ICU Medical, Inc. recalls ICU Medical Cogent Hemodynamic Monitoring System, Cogent Item Number 58400-000, UDI: (01)00840619079499
ICU Medical recalls Cogent Hemodynamic Monitoring System with software issues that may cause inaccurate readings, unit shutdowns, or loss of secondary parameter display. Affected units include specific serial numbers and software versions.
ICU MedicalJul 12, 2019 - UnratedMedical device
Ralston Group recalls Maximum Pelvic Trainer (MPT)
Ralston Group recalls Maximum Pelvic Trainers (MPT) due to FDA misbranding and lack of 510(k) submission. Affected units include specific lot numbers listed in the recall notice.
Ralston GroupJul 12, 2019 - Lower riskMedical device
Randox Laboratories Ltd. recalls This is an in vitro diagnostic product intended for use as a calibration serum in clinical chemistry assays. Randox
Rando: Randox recalls calibration serum (lot 961UE+) with potential 10% AST and 9% ALT errors affecting clinical tests. No remedy stated in official notice.
RandoxJul 12, 2019 - UnratedDrug
H J Harkins Company Inc dba Pharma Pac recalls Neomycin 3.5 mg/g / Polymyxin B10000 USP Units/g / Dexamethasone 1 mg/g Ophthalmic Ointment, 3.5 g tube, Rx only,
Pharma Pac recalls Neomycin 3.5 mg/g ophthalmic ointment due to insufficient quality assurance controls in manufacturing. This product was sold with specific lot numbers and expiration dates.
Pharma PacJul 12, 2019
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