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.

33151–33175 of 50502

  • HighFDA (Devices)·Z-1170-2017·2017-03-01

    Biomet Recalls Oxford Knee Instruments Due to Material Inclusions

    Biomet U.K., Ltd. is recalling Oxford Unicompartmental Knee Phase 3 Shim Size 1 instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Unicompartmental Knee Phase 3 Shim Size 1 Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Devices)·Z-1158-2017·2017-03-01

    Biomet Recalls Oxford Knee Instruments Due to Material Inclusions

    Biomet is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Partial Knee System Right Medial Tibial Trial Tray Size A Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • HighNHTSA·17V127000·2017-03-01

    Volvo Recalls 2017 Models for Side Air Bag Inflator Defect

    Volvo is recalling 2017 S60, V60, and XC60 vehicles because side air bag inflators may fail to ignite, preventing deployment in a crash.

    Product
    VOLVO — VOLVO V60, XC60, S60, V60CC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1169-2017·2017-03-01

    Biomet Recalls Oxford Knee Instruments Due to Material Inclusions

    Biomet U.K., Ltd. is recalling Oxford Knee instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Unicompartmental Knee Phase 3 Shim Size 2 Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Devices)·Z-1154-2017·2017-03-01

    Biomet Recalls Oxford Knee Instruments Due to Material Inclusions

    Biomet U.K., Ltd. is recalling Oxford Knee instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Unicompartmental Knee Phase 3 Tibial Impactor Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Devices)·Z-1229-2017·2017-03-01

    Philips Efficia CMS200 Central Monitoring System Recalled for Pediatric Alarm Defect

    Philips is recalling 156 Efficia CMS200 central monitoring systems because they may not alarm appropriately for pediatric or neonatal patients.

    Product
    Philips Efficia CMS200 Central Monitoring System; 863352 The Efficia CMS200 central monitoring system is intended for use by healthcare professionals for central viewing of physiologic waves, parameters, and trends from other networked medical devices (patient monitors and…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1233-2017·2017-03-01

    Degania Silicone Jackson-Pratt Drain Recalled for Sterility Compromise

    Degania Silicone is recalling 3,040 units of Jackson-Pratt Channel Drain Silicone Round because the sterile barrier was breached, compromising sterility.

    Product
    Jackson-Pratt Channel Drain Silicone Round, Fully Fluted w/10FR Trocar. Sterile. Rx Distributed by Cardinal Health, USA Catalog Number: JP-2187 For wound drainage.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-1162-2017·2017-03-01

    Biomet Oxford Partial Knee Instruments Recalled for Material Inclusions

    Biomet is recalling Oxford Partial Knee instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Partial Knee System Right Medial Tibial Trial Tray Size D Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Devices)·Z-1160-2017·2017-03-01

    Biomet Oxford Knee Instruments Recalled for Material Inclusions

    Biomet is recalling Oxford Partial Knee instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Partial Knee System Right Medial Tibial Trial Tray Size E Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • HighNHTSA·17V129000·2017-03-01

    Forest River Recalls 2017 Rockwood and Flagstaff Trailers for Tire Defect

    Forest River is recalling 2017 Rockwood and Flagstaff recreational trailers because a slide room bracket may damage the front tire, causing deflation and increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER ROCKWOOD, FLAGSTAFF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1166-2017·2017-03-01

    Biomet Oxford Partial Knee Instruments Recalled for Material Inclusions

    Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Partial Knee System Right Medial Tibial Trial Tray Size B Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Devices)·Z-1168-2017·2017-03-01

    Biomet Recalls Oxford Knee Instruments Due to Material Inclusions

    Biomet U.K., Ltd. is recalling Oxford Unicompartmental Knee Phase 3 Shim Size 3 instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Unicompartmental Knee Phase 3 Shim Size 3 Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Food)·F-1514-2017·2017-03-01

    Hostess Recalls Holiday White Peppermint Twinkies Due to Salmonella Risk

    Hostess Brands is recalling Holiday White Peppermint Twinkies because an ingredient may be contaminated with Salmonella. The product was distributed nationwide.

    Product
    Holiday White Peppermint Hostess Twinkies, cream-filled snack cakes, Net Wt. 13.02 oz. (369 g), UPC 888109111571.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1155-2017·2017-03-01

    Biomet Recalls Oxford Partial Knee Instruments Due to Material Inclusions

    Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Partial Knee System Phase 3 Tibial Template Right Medial Size A Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Devices)·Z-1153-2017·2017-03-01

    Biomet Oxford Knee Instruments Recalled for Potential Material Inclusions

    Biomet U.K., Ltd. is recalling Oxford Partial Knee System Femoral Slap Hammers due to potential alumina inclusions that could cause the instruments to crack or separate.

    Product
    Oxford Partial Knee System Femoral Slap Hammer Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Devices)·Z-1171-2017·2017-03-01

    Biomet Oxford Partial Knee Instruments Recalled for Material Inclusions

    Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Partial Knee System Phase 3 Tibial Template Right Medial Size D Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Devices)·Z-1156-2017·2017-03-01

    Biomet Oxford Partial Knee Instruments Recalled for Material Inclusions

    Biomet U.K. is recalling Oxford Partial Knee instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Partial Knee System Right Medial Tibial Trial Tray Size F Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Devices)·Z-1175-2017·2017-03-01

    Biomet Oxford Knee Instruments Recalled for Material Inclusions

    Biomet is recalling Oxford Knee instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Partial Knee System Phase 3 Tibial Template Right Medial Size B Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Food)·F-1530-2017·2017-03-01

    Mahatma Broccoli and Cheese Rice Recalled for Foreign Metal Material

    Riviana International is recalling Mahatma Broccoli & Cheese Rice due to the potential presence of foreign metal material.

    Product
    Mahatma Broccoli & Cheese Rice; 4 oz. net weight (UPC 17400-10529); packed 12 units in each case (sold as individual retail units). Shelf life is 18 months
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-1234-2017·2017-03-01

    Custom Medical Specialties Recalls Biopsy Trays with Syringes Due to Sterility Concerns

    Custom Medical Specialties is recalling 80 biopsy trays containing syringes because the sterility of the syringes could not be assured. The affected products were distributed to Idaho and Oregon.

    Product
    CMS-2193-R7 and CMS-1911-R3 Custom Biopsy Tray containing a BD 10cc LL Syringe, Sterile, Manufactured for CMS Custom Medical Specialties, Inc.
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-1163-2017·2017-03-01

    Biomet Recalls Oxford Knee Instruments Due to Material Inclusions

    Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Partial Knee System Left Medial Tibial Trial Tray Size D Product Usage: Instruments for use with the Oxford Uni Partial Knee System
    Category
    Medical Device
    Distribution
    14 states
  • HighCPSC·17099·2017-02-28

    Dillard's Recalls Baby Faux-Fur Coats Due to Choking Hazard

    Dillard's is recalling about 1,800 baby faux-fur coats because metal snaps can detach, posing a choking hazard to children.

    Product
    Faux-Fur Hooded Bear Coats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V121000·2017-02-27

    Tiffin Recalls 2012 Phaeton Motorhomes Due to Exhaust Fire Risk

    Tiffin is recalling 35 model-year 2012 Phaeton motorhomes because the exhaust pipe is mounted too close to the floor, creating a fire hazard.

    Product
    TIFFIN — TIFFIN PHAETON
    Category
    Vehicle
    Distribution
    Distributed nationwide