The Recall Desk

Hazard

Shelf Life recalls

74 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
74
Critical
0
Severe
0
Most recent
2026-04-15

Of the 74 shelf life recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all shelf life recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

26–50 of 74

  • ModerateFDA (Devices)·Z-2265-2025·2025-08-13

    T4 Total ELISA kit box expiry exceeds the standards' shelf life

    T4 Total ELISA kits are being recalled because the expiration date on the kit box label and Certificate of Analysis exceeded the shelf life of the standards and control solutions by two months. 47 units affected.

    Product
    Brand Name: T4 Total ELISA Product Name: T4 Total ELISA Model/Catalog Number: EIA-4568 Product Description: T4 Total ELISA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2191-2020·2020-06-10

    Osteomed Recalls Osteovation RMX Injectable Due to Shelf-Life Labeling Error

    Osteomed, LLC is recalling 651 units of Osteovation RMX 10 CC Injectable bone void filler kits because the labeled shelf-life may be incorrect, potentially affecting the product's setting characteristics.

    Product
    OSTEOVATION RMX 10 CC Injectable. REF/UDI: 390-6002/ /00813845021099 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2188-2020·2020-06-10

    Osteomed Recalls Osteovation 5cc Impactformula Bone Void Filler Kits

    Osteomed is recalling Osteovation 5cc Impactformula bone void filler kits because the product may not maintain its setting characteristics for the labeled shelf-life duration.

    Product
    OSTEOVATION 5CC IMPACTFORMULA. REF/UDI: 390-2105/00813845020085 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0558-2020·2019-12-04

    Boston Scientific Recalls Pancreatic Stents Due to Incorrect Shelf Life Labeling

    Boston Scientific is recalling 66 units of Advanix Pancreatic Stents because they were labeled with a 36-month shelf life instead of the approved 18-month shelf life.

    Product
    Boston Scientific Advanix Pancreatic Stent, Straight Leading Barb, 10F x 13cm UPN: M00536710
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3031-2018·2018-09-19

    SPS Sterilization Recalls Avid Venous Drainage Cannulas Due to Shelf Life Labeling

    SPS Sterilization is recalling 5 units of Avid Dual Stage Venous Drainage Cannulas because the expiration date on the label exceeds the validated shelf life.

    Product
    Edwards Lifesciences Avid Dual Stage Venous Drainage Cannula, 29/37F (9.6/12.3MM) X 37CM (14.5"), resterilized.
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-3035-2018·2018-09-19

    SPS Sterilization Recalls Boston Scientific Wallstent Due to Expiration Date Error

    SPS Sterilization is recalling two Boston Scientific Wallstent devices because the expiration date on the label exceeds the validated shelf life.

    Product
    Boston Scientific Wallstent Endoprosthesis Tracheobronchial Transhepatic Biliary Self-Expanding Stent, 12MM X 90MM | 75CM L, resterilized.
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-3040-2018·2018-09-19

    SPS Sterilization Recalls Boston Scientific Wallstent RP Endoprosthesis Due to Labeling Error

    SPS Sterilization, Inc. is recalling three Boston Scientific Wallstent RP Endoprosthesis tracheobronchial stents because the expiration date on the labeling exceeds the validated shelf life.

    Product
    Boston Scientific Wallstent RP Endoprosthesis Tracheobronchial Self-Expanding Stent, 10MM X 94MM | 135CM, resterilized.
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-3039-2018·2018-09-19

    SPS Sterilization Recalls Resterilized Boston Scientific Wallstent RP Endoprosthesis

    SPS Sterilization is recalling two units of resterilized Boston Scientific Wallstent RP Endoprosthesis because the labeling expiration date exceeds the validated shelf life.

    Product
    Boston Scientific Wallstent RP Endoprosthesis Tracheobronchial Transhepatic Biliary Self-Expanding Stent, 8MM X 80MM | 75CM, resterilized.
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-3030-2018·2018-09-19

    SPS Sterilization Recalls Edwards Venous Drainage Cannulas Due to Labeling Error

    SPS Sterilization is recalling five units of Edwards Lifesciences venous drainage cannulas because the expiration date on the label exceeds the validated shelf life.

    Product
    Edwards Lifesciences Thin-Flex Single Stage Venous Drainage Cannula, 34F (11.3MM) X 40CM (16"), resterilized.
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-1286-2018·2018-04-11

    Arrow Radial Artery Catheterization Kits Recalled for Shelf Life Labeling

    Arrow International is recalling Radial Artery Catheterization Kits because the included povidone iodine prep pads do not meet the 36-month shelf life requirement and should be labeled with a 24-month shelf life.

    Product
    Radial Artery Catheterization Kit; Model: AK-04220
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1285-2018·2018-04-11

    Arrow Radial Artery Catheterization Kits Recalled for Shelf Life Labeling Error

    Arrow International is recalling 570 Radial Artery Catheterization Kits because the included povidone iodine prep pads are labeled with an incorrect 36-month shelf life.

    Product
    Radial Artery Catheterization Kit; Model: AK-04122
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1087-2018·2018-03-28

    Centurion Minor Dressing Change Tray Recalled for Iodine Assay Failure

    Centurion Medical Products is recalling Minor Dressing Change Trays because a PVP Prep Pad component failed to meet required iodine assay levels for shelf life.

    Product
    MINOR DRESSING CHANGE TRAY
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1080-2018·2018-03-28

    Centurion Medical Products Recalls General Purpose Instrument Trays

    Centurion Medical Products is recalling General Purpose Instrument Trays because a PVP Prep Pad in the kit does not meet required iodine levels for shelf life.

    Product
    GENERAL PURPOSE INSTRUMENT TRAY
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0937-2018·2018-03-21

    Randox Liquid Cardiac Control CQ5053 Recalled for Shelf-Life Labeling Error

    Randox is recalling 450 kits of Liquid Cardiac Control CQ5053 because the product does not meet its shelf-life claim, potentially causing test results to fall outside control ranges.

    Product
    Liquid Cardiac Control CQ5053
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1918-2017·2017-05-10

    Smith & Nephew Recalls Renovation Thin Osteotome Blades Due to Shelf Life Data

    Smith & Nephew is recalling Renovation Thin Osteotome Blades because stability data does not support the labeled 10-year shelf life.

    Product
    RENOVATION, THIN OSTEOTOME BLADE, 10 MM X 3 INCH, REF 71369410, STERILE R, QTY: (1)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1911-2017·2017-05-10

    Smith & Nephew Recalls Radial Osteotome Blades Due to Shelf Life Data

    Smith & Nephew is recalling 1,126 units of Renovation Radial Osteotome Blades because stability data does not support the labeled 10-year shelf life.

    Product
    RENOVATION, RADIAL OSTEOTOME BLADE, SIZE 14, REF 71369314, STERILE R, QTY: (1)
    Category
    Medical Device
    Distribution
    Distributed nationwide