The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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35951–35975 of 40449

  • ModerateFDA (Devices)·Z-1497-2014·2014-04-30

    Teleflex Medical Recalls Non-absorbable Steel Sutures for Diameter Defects

    Teleflex Medical is recalling specific lots of non-absorbable steel sutures because they did not meet minimum diameter requirements.

    Product
    Monofilament and Multifilament Non-absorbable Steel Suture; Product Codes: 0520197-2, 29-727, 29-7270M4, 29-7281M4, E29-5553M4, E29-7270M4, E29-7272M4, E29-727A, EP4013P, EP4110N, X-2235, X29-7271M2, X-5667M8 and X-6730M5.
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-1496-2014·2014-04-30

    Zimmer Trabecular Metal Hip Implant Shell Recalled for Missing Locking Ring

    Zimmer, Inc. is recalling 17 units of Trabecular Metal Modular Acetabular System shells because the locking ring was missing.

    Product
    TRABECULAR METAL MODULAR ACETABULAR SYSTEM, Shell with Cluster Holes, Porous 60mm. Catalog number 00-6202-060-22; Hip implant component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1485-2014·2014-04-30

    Merit Medical Recalls Mixed Hydrophilic Guide Wire Lots

    Merit Medical Systems is recalling 173 units of Laureate Hydrophilic Guide Wire due to a labeling discrepancy where the product was mixed with a different lot.

    Product
    Merit Laureate Hydrophilic Guide Wire, Catalog No. LWSTFS35260EX, Straight Tip Stiff Shaft, 0.035" (0.89mm), 260 cm (102").
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1499-2014·2014-04-30

    Meta Labs Recalls Mega-Gen Personal Lubricant Due to Unregistered Manufacturer

    Altasource LLC is recalling Mega-Gen His and Hers Personal Lubricant because the firm is not registered as a drug manufacturer.

    Product
    Mega-Gen His Personal Lubricant, 8 fl. oz., Meta Labs, UPC Code 80708-3; Mega-Gen Hers Personal Lubricant, 8 fl. oz., Meta Labs, UPC Code 80808-0 Product Usage: A topical gel that increases sexual excitement and pleasure.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1475-2014·2014-04-30

    BioMerieux Recalls ZYM B Reagent Due to Visual Defect and Activity Issue

    BioMerieux SA is recalling ZYM B Reagent (REF 70493) because a visual defect and activity issue can cause false negative results in microbiological tests.

    Product
    ZYM B Reagent (REF 70493). The ZYM B reagent is an additional test used to reveal the results of some miniaturized biochemical test included in the API strips. The API product line is a standardized system combining several biochemical tests, which enables group or species…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1504-2014·2014-04-30

    Siemens ACUSON X700 Ultrasound Systems Recalled for Data Error

    Siemens is recalling 490 ACUSON X700 ultrasound systems because previous patient data may replace current patient dates in reports.

    Product
    Siemens ACUSON X700 Ultrasound Systems with software version 1.0.00, 1.0.01, 1.0.02, 1.1.00 and 1.1.02. ultrasound imaging system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1491-2014·2014-04-30

    Abbott Molecular Recalls CEP 8 Probe Kits Containing Incorrect Probe

    Abbott Molecular is recalling 20 kits of CEP 8 SG ASR Probe that contained the wrong probe. The kits contained Vysis CEP 4 probe instead of the expected CEP 8 probe.

    Product
    The CEP 8 SpectrumGreen (SG) ASR Probe Kit, 20ul (list 06J37-018) is an Analyte Specific Reagent (ASR) containing a single vial of CEP 8 spectrum green probe and a Certificate of Analysis (COA). Chromosome enumeration probes (CEP) are chromosome-specific FISH probes that…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1501-2014·2014-04-30

    Meta Labs Recalls Hot Ice Topical Gel Due to Unregistered Manufacturer

    Altasource LLC dba Meta Labs LLC is recalling 155 units of Hot Ice topical gel because the firm is not registered as a drug manufacturer.

    Product
    Hot Ice, 1 fl. oz., Meta Labs LLC, UPC 80705-2 Product Usage: A topical gel that increases men and womens secual excitement and pleasure.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1498-2014·2014-04-30

    FDA Recalls Amo-O Herbal Stimulator Gel for Unregistered Manufacturer

    Altasource LLC is recalling 70 units of Amo-O Herbal Stimulator gel because the firm is not registered as a drug manufacturer.

    Product
    Amo-O Herbal Stimulator, 2 fl. oz. Manufactured by Meta Labs, Alpharetta, GA 30076, UPC Code 80702-1 Product Usage: The product is a nonprescription, topical gel that is used to enhance libido and stimulate orgasmic pleasure.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1477-2014·2014-04-30

    BioMerieux Recalls ZYM B and FB Reagents Due to False Negative Results

    BioMerieux is recalling ZYM B and FB reagents because a visual defect and activity issue can cause false negative results in Rapid ID 32 strips and API biochemical tests.

    Product
    API NIH (REF 10400). ZYM B reagent is used and included inside of API NH (REF 10400) and API Listeria (10300). All of the API's are standardized systems combining several biochemical tests that enable group or species identification of most microorganisms.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1508-2014·2014-04-30

    Branan Medical ToxCup Drug Screen Cups Recalled for Labeling Errors

    Branan Medical is recalling ToxCup Drug Screen Cups because the lid labels may contain incorrect result interpretation graphics.

    Product
    ToxCup Drug Screen Cup, Catalogue Numbers: HT15, HT15A, PT11, PT11A, PT15A, PT23A, a screening device for the detection of drugs and drug metabolites in human urine. For in vitro diagnostic use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1502-2014·2014-04-30

    Varian On-Board Imager Elbow Motor Shaft Recall

    Varian Medical Systems is recalling On-Board Imager devices with Type 01 elbow motors due to a shaft failure caused by belt over-tensioning.

    Product
    On-Board Imager - Exact Arm Elbow Motor Shaft (kVD, kVS, and MV) with ''Type 01" elbow motors. Product Usage: The On-Board Imager device is an x-ray device used for evaluation of correct patient position in relation to isocenter and verification of treatment fields in…
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1487-2014·2014-04-30

    Boston Scientific Recalls iLab Ultrasound Systems Due to Measurement Error

    Boston Scientific is recalling 9 iLab Ultrasound Imaging Systems because a software update may cause the Longview distance measurement to display double the actual value.

    Product
    iLab Ultrasound Imaging System; iLab 3.0 (Polaris 1.0) software. Used for ultrasound examinations of intravascular pathology.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1490-2014·2014-04-30

    Ortho-Clinical VITROS Chemistry Calibration Data Module Recalled for Calibration Failure

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products CDM PROM No. 0168 because it lacks calibration parameters for DT CRSC slides, preventing system calibration.

    Product
    VITROS Chemistry Products CDM PROM (Calibration Data Module) No. 0168, Catalog Number/REF 199 9077, used in conjunction with: VITROS Chemistry Products CRSC DT Slides, Generation (GEN) 82, REF 6802721, and VITROS DT Calibrator Kit, Product Code 1957924, and tested on the VITROS…
    Category
    Medical Device
    Distribution
    10 states
  • ModerateFDA (Devices)·Z-1494-2014·2014-04-30

    Arrow Pressure Injectable PICC Catheter Recall Due to Incorrect Length

    Arrow International Inc. is recalling 789 units of Arrow Pressure Injectable PICC catheters because they contain a 40cm catheter instead of the required 50cm catheter.

    Product
    Arrow Pressure Injectable PICC Powered by Arrow VPS Stylet Catalogue number CDC-35052-VPS, peripherally inserted central catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1505-2014·2014-04-30

    Siemens Multix Fusion Radiographic System Recall for Loose Hose Holder

    Siemens is recalling 12 Multix Fusion radiographic systems because a corrugated hose holder may become loose. The issue requires verification and securing of the holder.

    Product
    MULTIX FUSION. The Multix Fusion system is a radiographic system used in hospitals, clinics, and medical practices. Multix Fusion enables radiographic exposures of the whole body including: skull, chest, abdomen, and extremities and may be used on pediatric, adult and…
    Category
    Medical Device
    Distribution
    8 states
  • CriticalFDA (Devices)·Z-1454-2014·2014-04-23

    FDA Recalls Alligator Retrieval Devices Due to Coating Delamination Risk

    Micro Therapeutics Inc is recalling Alligator Retrieval Devices because the PTFE coating may delaminate and detach from the delivery wire.

    Product
    Alligator Retrieval Device (ARD). Used in the peripheral and neurovasculature for foreign body removal.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1461-2014·2014-04-23

    Philips CT Scanners Recalled for Defective Service Latch Component

    Philips Medical Systems is recalling 135 CT scanners because a defective service latch component can cause the patient table top to become free-floating.

    Product
    Brilliance CT 16, Brilliance CT 64, Brilliance CT Big Bore Oncology, Brilliance CT Big Bore Radiology, Brilliance iCT, Ingenuity CT, Ingenuity Core, Ingenuity Core 128 and Ingenuity Flex scanners are Computed Tomography X-ray systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1453-2014·2014-04-23

    Ev3 Neurovascular Recalls Pipeline Embolization Devices Due to Coating Defect

    Ev3 Neurovascular is recalling 32 Pipeline Embolization Devices because the PTFE coating may delaminate and detach from the delivery wire.

    Product
    Pipeline Embolization Device (PED). Used endovascular treatment of adults with intracranial aneurysms in the internal carotid artery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1460-2014·2014-04-23

    Siemens AXIOM Vertix MD Trauma Systems Recalled for U-Arm Drop Risk

    Siemens is recalling two AXIOM Vertix MD Trauma systems because defective steel ropes may cause the U-arm to drop unexpectedly, posing a risk of serious injury to patients.

    Product
    AXIOM Vertix MD Trauma systems radiographic X-ray
    Category
    Medical Device
    Distribution
    2 states
  • SevereFDA (Devices)·Z-1442-2014·2014-04-23

    SpaceLabs Arkon Anesthesia Delivery System Recalled for Software Failure

    Del Mar Reynolds Medical is recalling 16 SpaceLabs Arkon Anesthesia Delivery Systems with Version 2.0 software because they may enter a controlled failed state.

    Product
    SpaceLabs Arkon Anesthesia Delivery System with Version 2.0 Software installed. This system includes a ventilator.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1467-2014·2014-04-23

    Edwards Lifesciences Recalls Fem-Flex II Arterial Cannulae Due to Tip Separation

    Edwards Lifesciences is recalling 28,885 Fem-Flex II Arterial and Femoral Cannulae because the dilator tips may separate.

    Product
    Edwards Lifesciences Fem-Flex II Arterial and femoral Cannulae with Duraflo Coating, arterial cannula sizes 16, 18 and 20 French, Models DFEMII016AS, DFEMII018AS, DFEMII020AS, DIIFEMII016A, DIIFEMII018A, and DIIFEMII020A.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1462-2014·2014-04-23

    GE OEC 9900 Elite Mobile Fluoroscopy System Recall for Monitor Fall Risk

    GE Healthcare is recalling 453 OEC 9900 Elite mobile fluoroscopy systems because defective screws may cause the workstation monitor to fall forward.

    Product
    The OEC 9900 Elite mobile fluoroscopy system (image intensified fluoroscopic x-ray) is designed to provide fluoroscopic and spot-film images of the patient during diagnostic surgical and interventional procedure. Examples of clinical application may include cholangiography…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1459-2014·2014-04-23

    CareFusion SmartSite Extension Set Recalled for Tubing Disconnections and Leaks

    CareFusion 303, Inc. is recalling 7,700 SmartSite Extension Sets due to disconnections and leakages at the tubing and Y-port connection.

    Product
    SmartSite Extension Set, Model No. 20029E, intravascular administration set.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1455-2014·2014-04-23

    Gambro Cartridge Blood Sets Recalled Due to Occluded Heparin Tubing

    Gambro Renal Products is recalling specific Gambro Cartridge Blood Sets because occluded heparin tubing may prevent anticoagulation dosing during hemodialysis.

    Product
    Gambro Cartridge Blood Set, blood transport system for hemodialysis, Model Number(s): 101025 (003410510) - Cartridge set, STND PRM LN and 103401 (003414500) - Cartridge set, PRM_LN_INJ_PT. The Gambro Cartridge Sets are single use sterile tubing sets intended to provide…
    Category
    Medical Device
    Distribution
    Distributed nationwide