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
34,891 found- Lower riskMedical device
CSL Behring GmbH recalls SIEMENS N/T Protein Control SL for use on the BN II, BN ProSpec Systems: N/T Protein Control SL/L: REF/Product Code
Siemens Healthcare recalls N/T Protein Control SL for Ceruloplasmin testing due to potential 20% lower results. Affected lots have incorrect value assignments. No remedy provided in recall notice.
Siemens HealthcareJun 5, 2017 - UnratedMedical device
Smiths Medical ASD Inc. recalls CADD(R) Medication Cassette Reservoir with clamp and female Luer. Non vented stopper included, REF 21-7002-24, Rx only,
Smiths Medical recalls CADD medication cassette reservoirs (REF 21-7002-24) with lot 16X659 due to potential incorrect pressure plate and tubing routing. Affected units may have safety issues.
Smiths MedicalJun 5, 2017 - Lower riskMedical device
Angiodynamics, Inc. recalls Accu2i pMTA Applicator, 19 cm INTERMEDIATE, REF/Catalog # 900-602-US, Model # (UPN) H787900602US0, STERILE --- This is
Angiodynamics recalls Accu2i pMTA Applicators with potential microwave energy failure due to coolant ingress causing error codes. Affected units include specific model numbers and lots.
AngiodynamicsJun 5, 2017 - Lower riskMedical device
Zimmer Biomet, Inc. recalls M/DN Intramedullary Fixation Humeral Guide Wire - Smooth 2.4 mm Diameter 70 cm Length Single Use Only, Item Number
Zimmer Biomet recalls certain humeral guide wires due to packaging configuration not covering 70cm wires. Affected items were sold before April 2:2022. No action needed as the issue is with packaging, not the product itself.
Zimmer BiometJun 5, 2017 - Lower riskMedical device
Zimmer Biomet, Inc. recalls RED SEXP DSTL FEM 19CM RT ASSY, model # CP111817
Zimmer Biomet recalls Red Sexp DSTL FEM 19CM RT Assay model CP111817 due to potential incorrect patient label in box. This may cause confusion during medical use. No action required as labels are otherwise correct.
Zimmer BiometJun 5, 2017 - Stop using nowDrug
Bristol-myers Squibb Company recalls EliquisTablets 5mg, 60 count bottle, Rx Only, Marketed by: Bristol-Meyers Squibb Company Princeton, NJ 08543 USA and
Bristol-Myers Squibb recalls Eliquis 5mg bottles due to a labeling error where lower-strength 2.5mg tablets were found inside.
EliquisJun 5, 2017 - Lower riskDrug
L. Perrigo Company recalls Walgreens Daytime and Nighttime Cold & Flu, packaged in combo pack of two plastic 12FL OZ (355 mL) bottles connected by
Walgreens Daytime and Nighttime Cold & Flu combo pack recalled due to incorrect product sleeve labeling. This mix-up means the product contains Day-Night Cough Liquid instead of Cold & Flu.
L. Perrigo CompanyJun 5, 2017 - Lower riskDrug
Apothecary By Design recalls Progesterone Injection in Olive Oil With Benzyl Alcohol 10%, 50mg/mL, 10mL Multi-Dose Vial, Rx only, Apothecary by
Apothecary By Design recalls progesterone injections with potential container closure issues that may affect product integrity. Affected units have specific lot numbers and expiration dates.
Apothecary By DesignJun 5, 2017 - Lower riskFood
Albertsons Inc recalls Carrot Cake Slice: Net Wt. 0 LB 7 OZ (198 g). Cake is assembled, iced, sliced and packaged at store level. Sliced
Albertsons recalls carrot cake slices due to missing walnuts in allergen statement. Nuts are visible through packaging. Consumers should check UPC code 0222132-0:000000 for affected products.
AlbertsonsJun 5, 2017 - Lower riskFood
Gilster-Mary Lee Corp. recalls Western Family Onion Soup Mix, 2.25 oz. pouches packaged in 4.5-oz. cartons
Western Family recalls onion soup mix pouches that may contain undeclared egg. Consumers should check product labels and contact the company for details.
Western FamilyJun 5, 2017 - Use cautionVehicle
MITSUBISHI OUTLANDER SPORT (2016) recall — Latches/Locks/Linkages
Mitsubishi recalls 2016 Outlander Sport vehicles with door latches that may not secure in high heat, risking door opening while driving. Owners must contact MMNA for free latch replacement.
MitsubishiJun 4, 2017 - Use cautionVehicle
NISSAN VERSA (2012) recall — Air Bags
Nissan recalls 2012 Versa vehicles with potential for curtain and seat-mounted air bags to deploy unexpectedly if door is slammed, requiring free repairs by dealers.
NissanJun 3, 2017 - Use cautionVehicle
PRIME TIME CRUSADER (2017) recall — Equipment
Forest River is recalling 2017 Prime Time Crusader trailers with incorrect axle placard causing potential overload and crash risk. Owners must get corrected placard free.
Forest RiverJun 3, 2017 - Use cautionVehicle
INFINITI QX30 (2017) recall — Air Bags
Nissan is recalling 2017 Infiniti QX30 vehicles with driver-side curtain air bags that may fail to deploy in crashes, increasing injury risk. Owners will receive free replacement of the air bag assembly.
InfinitiJun 3, 2017 - Use cautionVehicle
HYUNDAI SANTA FE (2017) recall — Tires
Hyundai recalls 2017 Santa Fe Sport vehicles with faulty tire pressure monitoring systems that may not warn of underinflated tires, increasing crash risk. Owners must have TPMS sensors replaced free by dealers.
HyundaiJun 3, 2017 - Use cautionMeat & poultry
P&S Bakery, Inc. Recalls Pepperoni Product Due to Possible Foreign Matter Contamination
P&S Bakery recalls 2,959 pounds of pepperoni rolls that may contain clear meat casing. Consumers are urged not to consume the product and should discard or return it.
P&S BakeryJun 2, 2017 - Use cautionMeat & poultry
Correctional Industries Airway Heights Food Operations Recalls Frozen Meat and Poultry Products Due to Water Contamination
USDA FSIS recalls 319,000 pounds of frozen meat and poultry products due to water contamination with PFOS/PFOA chemicals. Consumers urged not to consume these products.
Correctional Industries Airway Heights Food OperationsJun 2, 2017 - Lower riskMedical device
Sterilmed Inc recalls St. Jude Medical. Agilis NxT Steerable Introducer: B1-Directional, Medium Curl 22.4 mm, 71 cm, 6.5 F ID; Dilator: 94
St. Jude Medical recalls specific Agilis NxT Steerable Introducer models due to inadequate seal from lack of adhesive glue. Affected units include model STJ408309 and others with expiration dates prior to 05/31/2018.
St. Jude MedicalJun 2, 2017 - Lower riskMedical device
C.R. Bard, Inc. recalls Arctic Sun ArcticGel Pads - Medium, Product Code 317-07
C.R. Bard recalls Arctic Sun ArcticGel Pads (Product Code 317-07) due to incorrect box labeling. This may cause confusion but does not pose a safety risk.
C.R. BardJun 2, 2017 - Lower riskMedical device
C.R. Bard, Inc. recalls BARD DISPOZ-A-BAG Leg Bag with Flip-Flo Valve with Drain Extension, Extension Tube and Latex Straps, 19 oz. Packaged as
C.R. Bard recalls leg bags with flip-flo valve that may have cuts in the sterile barrier, risking infection. Check product code 151919 for affected units.
C.R. BardJun 2, 2017 - Use cautionMedical device
St. Jude Medical, Inc. recalls Infinity 7, Implantable Pulse Generator, REF 6663, Rx only, STERILE EO Product Usage: The Infinity IPG is an electronic
St. Jude Medical recalls Infinity 7 implantable pulse generators (REF 6663) due to potential loss of neuromodulation therapy when exposed to monopolar electrosurgical devices during medical procedures.
St. Jude MedicalJun 2, 2017 - Stop using nowDrug
G & W Laboratories, Inc. recalls G & W Clobetasol Propionate Ointment 0.05%, packaged in a) 15 g tube (NDC 0713-0656-15), b) 30 g tube (NDC
G & W Laboratories recalls 0.05% Clobetasol Propionate Ointment due to impurities that could cause harm. Affected lots include specific tube sizes and expiration dates. Stop using immediately.
G & W LaboratoriesJun 2, 2017 - Stop using nowFood
Ardent Mills, LLC recalls PRIMO MOLINO ITALIAN STYLE ENRICHED FLOUR, 50 lb, Packaged in paper bags, Store at Ambient Temperature, produced on
Ardent Mills recalls 50lb Italian style enriched flour (lot 6305SK) due to potential E. coli O121 contamination. Consumers should avoid using this product to prevent foodborne illness.
Ardent MillsJun 2, 2017 - Lower riskFood
Star Snacks Co., Llc. recalls Southern Grove Cashew Halves & Pieces with Sea Salt, Net Weight 8.0 oz. (227 grams)
Star Snacks recalls 8oz cashew halves with sea salt due to glass fragments found in some products. Consumers should check UPC code 041498179366 and discard if affected.
Star SnacksJun 2, 2017 - Lower riskFood
Kroger Corporate Food Technology Laboratory recalls BAKEHOUSE BREAD ARTISAN CRANBERRY ORANGE BREAD, 16 OZ UPC 8 64934 00004 4 Bakehouse Bread Company Tucson, AZ
Kroger recalls Cranberry Orange Bread (16oz) due to missing tree nut allergy warning. Check UPC 864934000044 for affected items sold June 2017 or earlier.
Bakehouse BreadJun 2, 2017 - Use cautionVehicle
FISKER KARMA (2012) recall — Air Bags
Recall of 2012 Fisker Karma vehicles with air bag inflators that may rupture during crashes, causing serious injury or death. Owners must have inflators replaced free by dealers.
Fisker KarmaJun 1, 2017 - Use cautionVehicle
KIA OPTIMA (2016) recall — Air Bags
Kia recalls one 2016 Optima vehicle due to potential air bag not inflating fully in crashes, increasing injury risk. Owners should contact Kia customer service for remedy.
KiaJun 1, 2017 - Lower riskMedical device
Solta Medical Inc recalls VASER Amplifier, VASER 2.2 VASERlipo System, Rx Only, 115/230V - 60/50Hz 300VA The Vaser amplifier is intended for the
Solta Medical recalls VASER Amplifiers and systems from 2016-2017 due to potential inaccurate calibration after service, risking patient burns. Affected units were serviced between September 2016 and May 2017.
Solta MedicalJun 1, 2017 - Lower riskMedical device
Boston Scientific Corporation recalls Boston Scientific Extractor Pro RX-S Retrieval Balloon Catheter 12-15mm Below UPN: M00547340
Boston Scientific recalls 12-15mm Below Extractor Pro RX-S catheters with incorrect injection location labeling that could lead to improper use. Affected units have UPN M00547340 and lot 19343:19343209 expiring 6/3/2018.
Boston ScientificJun 1, 2017 - Use cautionMedical device
Becton Dickinson & Co. recalls BD PhoenixTM AP, Catalog Number 448010 The BD Phoenix" AP instrument is designed for use with the BD Phoenix" system is
Becton Dickinson recalls BD Phoenix AP instruments with specific serial numbers due to potential unintended movement of the robot arm. This could affect lab use and requires immediate attention.
Becton DickinsonJun 1, 2017
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