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
35,004 found- Use cautionVehicle
WESTERN STAR 4900 (2020) recall — Structure
Daimler Trucks North America recalls 2017-2020 Western Star 4900 trucks due to risk of baggage/sleeper doors separating while moving, potentially causing injuries or crashes.
Daimler Trucks North AmericaOct 10, 2019 - Lower riskMedical device
Biocare Medical, LLC recalls 4plus Streptavidin HRP Label, Conjugated Streptavidin Horseradish Peroxidase, Detection Component, Catalog Number:
Biocare Medical recalls 4plus Streptavidin HRP Label (HP604H) due to potential invalid test results. This may cause patient tissue consumption and delayed diagnosis. Affected units have specific lot numbers.
Biocare MedicalOct 10, 2019 - Lower riskMedical device
Trilliant Surgical, LLC recalls 3.5mm Aresenal Screw Drill Bit , Ref: 330-35-001, Qty. 70, Rx Only, Non-Sterile, UDI: (01)00812926029696 - Product
Trilliant Surgical recalls 70 units of 3.5mm Aresenal Screw Drill Bits with labeling error that may cause misidentification and traceability issues. Affected items have specific lot numbers.
Trilliant SurgicalOct 10, 2019 - Lower riskMedical device
Hologic, Inc recalls Panther Fusion Extraction Reagent-S, Ref PRD-04331, IVD, CE, Rx Only consisting of FCR-S Fusion Capture Reagent - S,
Hologic recalls Panther Fusion Extraction Reagent-S (lot 258402) due to potential false positive/negative flu test results. Affected users should contact for remedy.
HologicOct 10, 2019 - Lower riskMedical device
Zimmer Biomet, Inc. recalls BF Humeral Stem, Various Sizes, Item Nos. 00430000606 00430000613 00430000706 00430000713 00430000813 00430000817
Zimmer Biomet recalls certain humeral stems (manufactured before Jan 2014) due to risk of implants adhering to LDPE packaging. Affected items have specific item numbers. No action needed if not in the list.
Zimmer BiometOct 10, 2019 - UnratedDrug
Innoveix Pharmaceuticals Inc recalls Lyophilized Human Chorionic Gonadotropin 5,500 USP Units For injection, Rx Only, Compounded by: Innoveix Addison, TX
Innoveix Pharmaceuticals recalls compounded Lyophilized Human Chorionic Gonadotropin 5,500 USP Units for injection due to lack of sterility assurance. This affects specific lots manufactured in Addison, TX. Contact for details.
InnoveixOct 10, 2019 - Lower riskFood
Dollar General Corporation recalls Sweet Smiles brand Select Dark Chocolate with Orange Peel Bar in 3.5 oz. foil wrapper packaging.
Dollar General's Sweet Smiles Select Dark Chocolate with Orange Peel Bar (3.5 oz) may contain undeclared milk allergen. Consumers should check product label for recall details.
Sweet SmilesOct 10, 2019 - Use cautionConsumer product
Carrier Recalls Carrier- and Bryant-Branded Heat Pumps Due to Fire Hazard
Carrier and Bryant recall 1.5-ton and 4-ton ductless heat pumps due to fire risk from overheating fan motors. Affected units require immediate repair to prevent fire.
Carrier & BryantOct 10, 2019 - Lower riskMedical device
Signature Orthopaedics Europe Ltd recalls Encina HA Femoral Stem, Size 11 Coxa Vara Collared, REF 100-30-011, Ti6AI4V Allow with HA Coating, For use with Stinson
Signature Orthopaedics Europe Ltd recalls Encina HA Femoral Stem (Size 11) due to mislabeled packaging causing surgical delays. Affected patients should contact the manufacturer for details.
Signature OrthopaedicsOct 9, 2019 - UnratedMedical device
Draegar Medical Systems, Inc. recalls Infinity M300 telemetry monitoring device Software versions VG2.3.1 and lower, Model Numbers MS25755, MS26076, MS26031,
Draegar recalls Infinity M300 telemetry monitoring devices with software versions VG2.3.1 and lower due to cybersecurity vulnerabilities including DDoS, spoofing, and tampering risks.
DraegarOct 9, 2019 - Lower riskMedical device
Stryker Sustainability Solutions recalls Zimmer Tourniquet Cuff 30" (Blue), PLC Dual Port, Single Bladder, Item Number: 60-7070-105, UDI: 00885825013868,
Stryker recalls blue 30" Zimmer tourniquet cuffs with potential mislabeling that could cause improper use or inadequate limb compression during procedures.
StrykerOct 9, 2019 - Lower riskMedical device
Nextremity Solutions recalls Stratum Foot Plating System-NL LP Screw 3.5x50mm ST, sterile. Catalog Number: STRM-NL-3550ST - Product Usage: The
Nextremity Solutions recalls Stratum Foot Plating System NL LP Screw 3.5x50mm ST (lot M1151) due to possible incorrect screw type and length. Affected users should check their product details.
Nextremity SolutionsOct 9, 2019 - Use cautionMedical device
Medivators, Inc. recalls Medivators Endo Smartcap Endoscope Tubing. REF100145CO2EXTU, packaged as Contents 1, 10, 50. Tubing for Olympus
Medivators recalls Endo Smartcap Endoscope Tubing (REF100145CO2EXTU) due to potential inadequate insufflation, air bubbles, or water leakage during endoscopic procedures. Affected units include specific lot numbers and packaging sizes.
MedivatorsOct 9, 2019 - Stop using nowDrug
Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center recalls PF-Fentanyl Citrate 2 mcg/mL* & Bupivacaine HCl 0.125% in 0.9% Sodium Chloride Injection-250 mL, Rx Only Total Dose:
Nephron Pharmaceuticals recalls specific fentanyl and bupivacaine injections for potential glass contamination. Affected lots expired by December 2019. Contact for return instructions.
NephronOct 9, 2019 - Stop using nowDrug
Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center recalls Amino Acid Injection 50 g/1000 mL (50 mg/mL) 25 g L-Arginine HCl; 25 g L-Lysine HCl, Single Dose Container, Rx Only
Nephron Pharmaceuticals recalls specific amino acid injection due to potential leakage causing contamination. Affected units have NDC 69374-988-10 and lots AA9023A/AA9023B expiring 10/24/2019.
NephronOct 9, 2019 - Stop using nowDrug
Ingenus Pharmaceuticals Llc recalls Leucovorin Calcium Injection, USP 500 mg*/50 mL (10 mg/mL) 50 mL Single-Dose Vial NDC 50742-464-50 Rx Only Ingenus
Ingenus Pharmaceuticals recalls Leucovorin Calcium Injection vials with particulate matter risk. Affected lots expire April 2020 or later. Contact for return instructions.
IngenusOct 9, 2019 - Lower riskFood
Whole Foods Market recalls Whole Foods Market White Parkerhouse Rolls PLU 49557 NET WT. 0 lb 12 oz (340g) packaged in a clear plastic bag 12 rolls
Whole Foods Market recalls Parkerhouse Rolls due to undeclared milk and eggs. Consumers should check product labels for PLU 49557 and date.
Whole Foods MarketOct 9, 2019 - Lower riskMedical device
Roche Diagnostics Operations, Inc. recalls Cobas infinity central lab / cobas infinity core license-a Calculator/Data Processing Module, For Clinical Use Material
Roche recalls Cobas Infinity lab software versions 2.4.1 to 2.5.4 due to incorrect alarm mapping that could lead to missed clinical alerts.
RocheOct 8, 2019 - Use cautionMedical device
Avanos Medical, Inc. recalls CORFLO* Percutaneous Endoscopic Gastrostomy (PEG) Kit, Labeled as CORFLO* PEG Kit with ENFit Connector. 2 units per
Avanos Medical recalls 2 units of CORFLO PEG kits with ENFit connectors due to risk of guidewire not passing through the connector, potentially causing complications during medical procedures.
Avanos MedicalOct 8, 2019 - Use cautionMedical device
Teleflex Medical recalls Arrow EZ-IO Intraosseous Vascular Access System 25mm Needle+Stabilizer Kit, Product Code 9001P-VC-005 - Product Usage:
Teleflex Medical recalls Arrow EZ-IO Intraosseous Vascular Access System 25mm Needle+Stabilizer Kit due to safety cap dislodging, risking needle stick injuries and packaging contamination.
Teleflex MedicalOct 8, 2019 - Lower riskFood
Fisherman's Pride Processor, Inc. dba Neptune Foods recalls Schwan's Garlic Herb Shrimp NET WT 16 oz. (1 lb.) Keep Frozen Cook Thoroughly Distributed By: Schwan's Home Service,
Neptune Foods recalls Schwan's Garlic Herb Shrimp (16 oz) due to undeclared milk and soy lecithin allergens. Keep frozen and cook thoroughly to avoid allergic reactions.
Neptune FoodsOct 8, 2019 - Lower riskFood
Blue Bell Creameries, L.P. recalls Blue Bell Butter Crunch Ice Cream packaged in a 1/2 Gallon (2 Qts) paperboard cup & lid (4 units per corrugated sleeve,
Blue Bell Creameries recalls Butter Crunch Ice Cream in 1/2 gallon paper cups due to possible foreign material. Consumers should check product codes and contact Blue Bell for details.
Blue BellOct 8, 2019 - Stop using nowConsumer product
Ronson Brand Tech Torch Recalled by Zippo Due to Fire Hazard
Ronson Tech Torch Auto Start recalled due to flame continuing after trigger release. Stop using immediately and get refund via gift card.
RonsonOct 8, 2019 - Stop using nowConsumer product
Kawasaki Motors USA Recalls Lawn Mower Engines Due to Burn and Fire Hazards (Recall Alert)
Kawasaki recalls 2017-2018 riding lawn mower engines with fuel injector leaks that can cause burns and fires. Affected models include Ferris IS 2100Z ZTR and Cub Cadet Pro Z 760 LKW EFI. Consumers must stop using and contact Kawasaki for free repair.
KawasakiOct 8, 2019 - Stop using nowConsumer product
IKEA Recalls Infant Bibs Due to Choking Hazard
IKEA recalls MATVRÅ infant bibs for infants due to choking hazard from detachable snap. Return to store for full refund.
IKEAOct 8, 2019 - Use cautionVehicle
SUBARU ASCENT (2019) recall — Power Train
Subaru is recalling certain 2019 Ascent vehicles due to potential driveshaft disconnection that could increase crash risk. Owners will receive free replacement of driveshaft assembly and center support brace.
SubaruOct 7, 2019 - Use cautionVehicle
FORD RANGER (2019) recall — Seat Belts
Ford is recalling 2019 Ranger SuperCab vehicles with potentially improperly assembled front passenger seat belts that may not restrain occupants in crashes.
FordOct 7, 2019 - Lower riskMedical device
The Binding Site Group, Ltd. recalls Optilite Optilite Rheumatoid Factor Kit, Ref: LK151.OPT.A, IVD, Rx Only, UDI: 05051700020015 (kit ea. containing four
The Binding Site Group recalls Optilite Rheumatoid Factor Kit (UDI: 05051700020015) due to potential false positive results in rheumatoid arthritis testing, which may cause unnecessary tests and delayed treatment.
The Binding Site GroupOct 7, 2019 - Lower riskMedical device
Smith & Nephew, Inc. recalls LAG SCREW 3.2MM GUIDE PIN SLEEVE, REF 71674032 - Product Usage: The TRIGEN InterTAN nails are indicated for fractures
Smith & Nephew recalls LAG screw 3.2mm guide pin sleeves (ref 71674032) due to manufacturing error causing detent balls to not fully compress. Affected batch numbers include 18DM11613A, 18HM02575, 18HM13327A, 18HM20956A.
Smith & NephewOct 7, 2019 - Use cautionMedical device
Edwards Lifesciences, LLC recalls Oxymetry Cable, Rxonly. REF/UDI: HEMOXSC100/(01)00690103196986 - Product Usage: The HemoSphere oximetry cable is a
Edwards Lifesciences recalls specific oxymetry cables due to inconsistent crimping causing intermittent communication issues. Affected cables have listed serial numbers; stop using if you own one.
Edwards LifesciencesOct 7, 2019
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