The Recall Desk

Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

40676–40700 of 50511

  • HighNHTSA·14V512000·2014-08-20

    Autocar Recalls 2015 Xspotter Trucks Due to Fuel Filter Defect

    Autocar is recalling 19 model year 2015 Xspotter heavy-duty trucks because a fuel filter defect may cause the engine to stall without warning, increasing the risk of a crash.

    Product
    AUTOCAR — AUTOCAR XSPOTTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2210-2014·2014-08-20

    Medical Positioning Rapid Response HUT Table Recall for Malfunction Risk

    Medical Positioning Inc. is recalling 17 Rapid Response HUT tables because a defective component may cause the table to drop into the Trendelenburg position more rapidly than normal under excessive weight.

    Product
    Medical Positioning Rapid Response HUT table with Dual 2 Way Drop Section, Powered Medical Examination table, Model # 1217. Product Usage: Used to conduct syncope examinations.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2174-2014·2014-08-20

    Siemens Linear Accelerators Recalled for Potential Patient Collision Risk

    Siemens Medical Solutions is recalling 160 linear accelerators because automatic treatment movements could cause the machine to collide with patients.

    Product
    Siemens Linear Accelerators of type ARTISTE, ONCOR, and PRIMUS with Automatic Sequenced Cancer Treatment Delivery Option.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2172-2014·2014-08-20

    Medtronic Recalls Ascenda Intrathecal Catheters Due to Retainer Ring Defect

    Medtronic is recalling specific lots of Ascenda Intrathecal Catheters and Revision Kits because a retainer ring component may not meet specifications, risking catheter disconnection.

    Product
    Medtronic Ascenda Intrathecal Catheter models 8780 and 8781, and Ascenda Intrathecal Catheter Pump Segment Revision Kit, model 8784. The Ascenda Intrathecal Catheter is part of an infusion system that stores and delivers parenteral drugs to the intrathecal space. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2218-2014·2014-08-20

    Zimmer Recalls Double Offset Rasp Handles Due to Assembly Failure

    Zimmer, Inc. is recalling 412 Double Offset Rasp Handles because the handle may fail to remain assembled to the rasp during use.

    Product
    Double Offset Rasp Handle, Left Hand Nonsterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2207-2014·2014-08-20

    Gambro Recalls X-MARS Sets Due to Connector Breakage and Leakage

    Gambro Renal Products is recalling X-MARS Sets because connector breakages can cause leakage of liquid or blood.

    Product
    X-MARS Set (component of MARS Treatment Kit Type 1116/1 X-MARS US), Product Number 800541
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2232-2014·2014-08-20

    BioMerieux Recalls VIDAS D-Dimer Exclusion II Test Kits

    BioMerieux SA is recalling 2,160 units of VIDAS D-Dimer Exclusion II tests due to complaints of non-repeatable results that may cause false negatives.

    Product
    VIDAS D-Dimer Exclusion II, an automated quantitative test for use on instruments of the VIDAS family for the immunoenzymatic determination of fibrin degradation products in human plasma using the Enzyme Linked Fluorescent Assay technique. Also indicated for use in conjunction…
    Category
    Medical Device
    Distribution
    40 states
  • HighFDA (Devices)·Z-2205-2014·2014-08-20

    Gambro Recalls Prismaflex HF 1400 Dialysis Sets Due to Connector Breakage

    Gambro Renal Products is recalling Prismaflex HF 1400 dialysis sets because connector breakages can cause leakage of liquid or blood.

    Product
    Prismaflex HF 1400. Product number 107142. Each set is packaged in a plastic pouch, 4 pouches per carton box
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-2325-2014·2014-08-20

    Miceli Dairy Products Recalls Ricotta Cheese Due to Beta Lactam Residues

    Miceli Dairy Products is recalling Farimont Foods Ricotta Cheese because the whey protein concentrate used in manufacturing tested positive for beta lactam residues.

    Product
    Farimont Foods Ricotta Cheese packaged in 30 pound bags.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-2175-2014·2014-08-20

    Agfa Healthcare Recalls DX-D 600 Imaging Packages Due to Crane Movement

    Agfa Healthcare is recalling 17 DX-D 600 imaging packages because the overhead tube crane may move uncontrolled. Customers should stop using the equipment.

    Product
    DX-D 600 - DXD Imaging Package Product Usage:Is indicated for use in providing diagnostic quality images to aid the physician with diagnosis. Systems can be used with MUSICA2 image processing to create radiographic images of the skeleton including skull, spinal column and…
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Devices)·Z-2223-2014·2014-08-20

    Zimmer Recalls Nonsterile Orthopedic Rasps Due to Handle Failure

    Zimmer, Inc. is recalling 412 units of nonsterile orthopedic rasps because the handle may fail to remain assembled during use.

    Product
    Vl DBL OFFST WI LRG STPL, RT Nonsterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2211-2014·2014-08-20

    Medical Positioning Rapid Response HUT Table Recalled for Malfunction Risk

    Medical Positioning Inc. is recalling Model # 1219 HUT tables because a defective component may cause the table to drop rapidly into the Trendelenburg position under excessive weight.

    Product
    Medical Positioning Rapid Response HUT table, Powered Medical Examination table, Model # 1219. Product Usage: Used to conduct syncope examinations.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2198-2014·2014-08-20

    Gambro Recalls Prisma M100 Sets Due to Connector Breakage

    Gambro Renal Products is recalling Prisma M100 sets because connector breakages can cause liquid or blood to leak.

    Product
    Prisma M100 set. Product number 104182. Each set is packaged in a plastic pouch, 4 pouches per carton box
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2221-2014·2014-08-20

    Zimmer Recalls Double Offset Rasp Handles Due to Assembly Failure

    Zimmer, Inc. is recalling 412 nonsterile Double Offset Rasp Handles that may fail to remain assembled during use.

    Product
    Double Offset Rasp Handle, Left Hand Nonsterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2196-2014·2014-08-20

    Gambro Recalls Prisma M60 Postdilution Sets Due to Connector Breakage

    Gambro Renal Products is recalling Prisma M60 POSTDILUTION sets because connector breakages can cause leakage of liquid or blood.

    Product
    Prisma M60 POSTDILUTION set. Product number 104183. Each set is packaged in a plastic pouch, 4 pouches per carton box
    Category
    Medical Device
    Distribution
    0 states
  • HighCPSC·14258·2014-08-19

    Bexco Recalls Franklin & Ben Mason Cribs Due to Fall and Entrapment Hazards

    Bexco is recalling Franklin & Ben Mason 4-in-1 Convertible Cribs because the front panel can separate from the side panels, creating a gap that poses fall and entrapment risks to children.

    Product
    Franklin & Ben Mason 4-in-1 Convertible Cribs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V510000·2014-08-19

    Blue Bird School Bus Wheelchair Lift Platform Recall

    Blue Bird is recalling certain 2007-2015 school buses because wheelchair lift platform side plates may crack, posing an injury risk to operators.

    Product
    BLUE BIRD — BLUE BIRD VISION, ALL AMERICAN, MICRO BIRD, CONVENTIONAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14257·2014-08-19

    Brita Recalls Children's Water Bottles Due to Laceration Hazard

    Brita is recalling about 242,500 children's water filter bottles because the lids can break into sharp pieces, posing a laceration hazard. No injuries have been reported.

    Product
    Brita hard-sided water filter bottle for kids
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V511000·2014-08-19

    Blue Bird Recalls Non-School Buses with Cracking Wheelchair Lifts

    Blue Bird is recalling 90 non-school buses from 2007-2015 because wheelchair lift platform side plates may crack, posing an injury risk to operators.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN, VISION, MICRO BIRD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V509000·2014-08-19

    Starcraft RV Recalls 2015 Launch Travel Trailers Due to Tire Label Error

    Starcraft RV is recalling 12 model year 2015 16RB Launch travel trailers because the Federal ID label lists incorrect tire pressure, which could lead to a tire blowout.

    Product
    STARCRAFT RV TT — STARCRAFT RV TT LAUNCH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14E054000·2014-08-18

    Buyers Products Recalls Warning Triangles Due to Wind Instability

    Buyers Products is recalling warning triangles that may blow over in wind gusts, potentially failing to warn other drivers of a stopped vehicle.

    Product
    EQUIPMENT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14743·2014-08-14

    Arctic Cat Snowmobiles Recalled for Fuel Leak and Fire Hazard

    Arctic Cat is recalling about 3,260 model year 2014 and 2015 XF 7000 and ZR 7000 snowmobiles because the fuel line assembly can leak, posing a fire hazard.

    Product
    Arctic Cat snowmobiles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V498000·2014-08-13

    Ford F-Series Super Duty Trucks Recalled for Fire Risk

    PJ's Truck Bodies is recalling 2009-2013 Ford F-350, F-450, and F-550 trucks modified with specific PTO assemblies due to an oil leak that poses a fire risk.

    Product
    FORD — FORD F-550, F-450, F-350
    Category
    Vehicle
    Distribution
    Distributed nationwide