The Recall Desk

Severity 2 of 5

Moderate recalls

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

What “moderate” means here

Severity 2 (Moderate) recalls cover minor labeling errors, low-risk contamination, and voluntary precautionary recalls. The agency's own classification is typically FDA Class III, or the issue is something like incomplete instructions or a small UPC mismatch where the product itself is safe but doesn't meet documentation requirements. Use the same brand-name product safely; follow the manufacturer's instructions for return or exchange if you want a refund.

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.

11126–11150 of 21617

  • ModerateFDA (Devices)·Z-0705-2018·2018-03-07

    Teleflex Recalls Rusch Greenlite MAC 1 Tracheal Intubation Devices

    Teleflex Medical is recalling Rusch Greenlite MAC 1 devices because some pouches may contain the incorrect product size, specifically MAC 2 instead of MAC 1.

    Product
    Rusch Greenlite MAC 1, Catalog Number 004551001. Used during tracheal intubation.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Food)·F-0862-2018·2018-03-07

    Schmidt Baking Recalls 12 Grain Bread Due to Foreign Material Risk

    Schmidt Baking Co. is recalling 12 Grain bread products due to a potential foreign material contamination identified by a vendor.

    Product
    12 GRAIN ( Under the following Trade Names - O/T )
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-0790-2018·2018-03-07

    Avid Medical Recalls GYN Laparoscopy Kits With Foreign Material

    Avid Medical is recalling 160 GYN laparoscopy kits because they may contain needles with loose polypropylene foreign material.

    Product
    AVID TruCustom GYN LAPAROSCOPY convenience kits, Item Code: LGHM013-06 and LGHM013-07
    Category
    Medical Device
    Distribution
    10 states
  • ModerateFDA (Devices)·Z-0808-2018·2018-03-07

    Siemens Syngo.via Software Recall for Diagnostic Inconsistencies

    Siemens Medical Solutions is recalling 30 Syngo.via systems with software version VB20A to resolve bugs and inconsistent diagnoses.

    Product
    Syngo.via systems with SW VB20A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0545-2018·2018-03-07

    Allergan Recalls Iron Dextran Injection Due to Stability Failures

    Allergan is recalling INFeD (Iron Dextran Injection USP) because stability testing showed the product did not meet specifications for iron content.

    Product
    INFeD (Iron Dextran Injection USP) 100 mg elemental iron/2 ml (50 mg/mL), Rx Only, packaged in a) single dose vials, (NDC 52544-931-07), b) carton of 10 x 2 ml Single Dose Vials (NDC 52544-931-02) Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054, Manufactured by: Patheon
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0725-2018·2018-03-07

    Terumo Destination Guiding Sheath Recalled for Specification Deviation

    Terumo Medical Corporation is recalling 33 units of Destination Guiding Sheath catheter introducers because the tucking depth feature is marginally outside the upper specification.

    Product
    Destination Guiding Sheath catheter introducer, Catalog Number: RSR06 Product Usage: The Destination¿ Guiding Sheath is designed to be used for the introduction of interventional and diagnostic devices into the human vasculature, including but not limited to the renal, caroti
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0757-2018·2018-03-07

    Steris Recalls Vis-U-All High Temperature Sterilization Pouches Due to Ink Migration

    Steris Corporation is recalling Vis-U-All High Temperature Sterilization Pouches because purple ink on the exterior label may migrate during steam processing, causing cosmetic defects and potential ink transfer to medical devices.

    Product
    Vis-U-All High Temp 6"x10" Heat Seal Pouch 200 pouches per box; 5 boxes per case Product Usage: The Vis-U-All High Temperature Sterilization Pouch is suitable for use by healthcare providers to enclose and seal medical devices to be sterilized by steam. The pouch is designed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0709-2018·2018-03-07

    Siemens Medical Solutions Recalls Wireless Foot Switches for X-Ray Systems

    Siemens Medical Solutions is recalling wireless foot switches for Artis Q and Q.zen fluoroscopic systems because they may fail to release radiation due to external impacts.

    Product
    Artis Q and Q.zen model Interventional fluoroscopic x-ray system wireless foot switch accessory; Model Numbers: 4787797, 4787805, and 4787813.
    Category
    Medical Device
    Distribution
    52 states
  • ModerateFDA (Devices)·Z-0761-2018·2018-03-07

    Steris Recalls Vis-U-All High Temperature Sterilization Pouches Due to Ink Migration

    Steris Corporation is recalling Vis-U-All High Temperature Sterilization Pouches because purple ink on the exterior label may migrate during steam processing, causing cosmetic defects and potential ink transfer to medical devices.

    Product
    Vis-U-All High Temp 3.5"x9" Self Seal Pouch 200 pouches per box; 4 boxes per case Product Usage: The Vis-U-All High Temperature Sterilization Pouch is suitable for use by healthcare providers to enclose and seal medical devices to be sterilized by steam. The pouch is designed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0873-2018·2018-03-07

    Meijer Recalls Greek Yogurt Due to Potential Glass Particles

    Meijer Distribution is voluntarily recalling select Greek and Low-fat yogurt products due to the potential risk of small glass particles.

    Product
    Meijer Greek Yogurt 0% Vanilla 5.3 oz. The products are packaged in a plastic cup with a foil seal and a label listing the above-mentioned UPCs.
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Food)·F-0870-2018·2018-03-07

    Meijer Greek Yogurt Recalled for Potential Glass Particles

    Meijer Distribution is voluntarily recalling select Greek and Low-fat yogurt products due to a potential risk of small glass particles.

    Product
    Meijer Greek Yogurt 0% Black Cherry 5.3 oz. The products are packaged in a plastic cup with a foil seal and a label listing the above-mentioned UPCs.
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-0781-2018·2018-03-07

    Avid Medical Recalls Vascular and Neuro Kits with Foreign Material

    Avid Medical is recalling 200 TruCustom DJ's Vascular/Neuro Tray kits because they may contain needles with loose polypropylene foreign material.

    Product
    AVID TruCustom DJ'S VASCULAR/NEURO TRAY convenience kits, Item Code: AV010930-12
    Category
    Medical Device
    Distribution
    10 states
  • ModerateFDA (Food)·F-0854-2018·2018-03-07

    Schmidt Baking Recalls Bread Products Due to Potential Foreign Material

    Schmidt Baking Co. is recalling various bread products sold under multiple trade names due to a potential foreign material issue identified by a vendor.

    Product
    P/L HAMS( Under the following Trade Names - CHERRY VALLEY, COMPARE, FINEFARE, GIANT, GOURMET, HP, HOLSUM, KEYFOODS, KRASDALE, METFOODS, PIONEER, REDNER, SHOPPERS, SUPERA, SUPERBREAD, TOP TOMATO, TRADEFAIR, WEIS, 7 ELEVEN, HAUWALD, GREAT VALUE, GENERIC, GOURMET 16CT, REDER 16CT,
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Food)·F-0852-2018·2018-03-07

    Schmidt Baking Recalls Lite Hams Due to Potential Foreign Material

    Schmidt Baking Co. is recalling Lite Hams sold under Gaint, ShopRite, and Weis brands due to a potential foreign material in an ingredient supplied by a vendor.

    Product
    LITE HAMS( Under the following Trade Names - GAINT, SHOPRITE, WEIS)
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Food)·F-0841-2018·2018-03-07

    Schmidt Baking Recalls Wheat Rolls Due to Potential Foreign Material

    Schmidt Baking Co. is recalling wheat rolls sold under four trade names due to a potential foreign material issue identified by a vendor.

    Product
    BNS WHEAT ROLLS ( Under the following Trade Names - Giant, Harvest Pride, Shoppers and Old Tyme )
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-0743-2018·2018-03-07

    Steris Recalls Vis-U-All High Temperature Sterilization Pouches Due to Ink Migration

    Steris Corporation is recalling Vis-U-All High Temperature Sterilization Pouches because purple ink on the exterior label may migrate during steam processing, causing cosmetic defects and potential ink transfer to enclosed devices.

    Product
    Vis-U-All High Temp 7.5"x13" Self Seal Pouch 200 pouches per box; 4 boxes per case Product Usage: The Vis-U-All High Temperature Sterilization Pouch is suitable for use by healthcare providers to enclose and seal medical devices to be sterilized by steam. The pouch is designe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0759-2018·2018-03-07

    Steris Recalls Vis-U-All Heat Seal Pouches Due to Ink Migration

    Steris Corporation is recalling Vis-U-All High Temp Heat Seal Pouches because purple ink on the exterior label may migrate during steam processing, causing cosmetic defects and potential ink transfer to medical devices.

    Product
    Vis-U-All High Temp 8"x10" Heat Seal Pouch 200 pouches per box; 5 boxes per case Product Usage: The Vis-U-All High Temperature Sterilization Pouch is suitable for use by healthcare providers to enclose and seal medical devices to be sterilized by steam. The pouch is designed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0863-2018·2018-03-07

    Schmidt Baking Recalls White Wheat Bread Due to Foreign Material Risk

    Schmidt Baking Co. is recalling specific white wheat bread products because a vendor ingredient may contain foreign material.

    Product
    WHITE WHEAT R/T ( Under the following Trade Names - O/T 2PK, O/T, WEIS, ULTRA GRAIN )
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-0765-2018·2018-03-07

    Steris Recalls Vis-U-All High Temperature Sterilization Pouches Due to Ink Migration

    Steris Corporation is recalling Vis-U-All High Temperature Sterilization Pouches because purple ink on the exterior label may migrate during steam processing, causing cosmetic defects and potential ink transfer to medical devices.

    Product
    Vis-U-All High Temp 10.5"x28" Self Seal Pouch 100 pouches per box; 4 boxes per case Product Usage: The Vis-U-All High Temperature Sterilization Pouch is suitable for use by healthcare providers to enclose and seal medical devices to be sterilized by steam. The pouch is design
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0720-2018·2018-03-07

    Siemens Recalls ADVIA Centaur T3 Kits Due to Barcode Scanning Issue

    Siemens is recalling ADVIA Centaur T3 kits because a barcode scanning issue on the ADVIA Centaur XPT system may affect specific lots.

    Product
    ADVIA Centaur¿ T3 ADVIA Centaur T3: For in vitro diagnostic use in the quantitative determination of triiodothyronine (T3) in serum using the ADVIA Centaur, ADVIA Centaur XP, and ADVIA Centaur XPT systems. Measurements of triiodothyronine are used in the diagnosis and treatmen
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Food)·F-0848-2018·2018-03-07

    Schmidt Baking Recalls White Wheat Hams Due to Potential Foreign Material

    Schmidt Baking Co. is recalling White Wheat Hams under OT, WEIS, and ULTRA GRAIN brands due to potential foreign material from a recalled ingredient.

    Product
    WHITE WHEAT HAMS( Under the following Trade Names - OT, WEIS, ULTRA GRAIN )
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-0718-2018·2018-03-07

    Keystone Dental Recalls Max Implant System Bone Taps Due to Mislabeling

    Keystone Dental Inc. is recalling 72 units of the Max Implant System Bone Tap because an 8mm diameter tap was incorrectly marked and labeled as 7mm.

    Product
    Max Implant System - Bone Tap for use with 7.0mm diameter Max Implant, Catalog Number D-TAP-MAX7-7 Dental implants are intended for use as anchors of fixed or semi-fixed dental crowns, bridges, and overdentures in patients with partial or full edentulism of the upper or lowe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0698-2018·2018-03-07

    Moog Curlin Infusion Set Recalled for Particulate Contamination

    Zevex Incorporated is recalling Moog Curlin Infusion Administration Sets because particulate matter was found on the spike.

    Product
    MOOG Curlin Infusion Administration Set, Ref 340-4133, Non-DEHP Microbore Tubing with Non-Vented Bag Spike and Needleless Injection Port (Positive Pressure), packaged 20/box, for use with the Moog Curlin Ambulatory Volumetric Infusion Pump, RX, Sterile. Product Usage: Admini
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0845-2018·2018-03-07

    Schmidt Baking Recalls Potato Bread Due to Potential Foreign Material

    Schmidt Baking Co. is recalling potato bread products under various trade names due to a potential foreign material in an ingredient supplied by a vendor.

    Product
    P/L POTATO ( Under the following Trade Names - WHOLE FOOODS, PLAIN BAG, GIANT, HP, SHOPPERS, SHOPRITE, WEIS )
    Category
    Food
    Distribution
    8 states