Hazard

Regulatory Non Compliance recalls

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

What the numbers show

Total: 536
Critical: 0
Severe: 56
Most recent: 2026-07-01

Of the 536 regulatory non compliance recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 56 (10%) are Severe.

Which agencies issued them

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all regulatory non compliance 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.

501–525 of 536

ModerateFDA (Devices)·Z-2204-2013·2013-09-25
Camlog USA Recalls Uncleared Dental Implant Abutments in Four States
Camlog USA is recalling one unit of a CONELOG Titanium Base dental implant abutment because it was not cleared for sale or use in the United States.
Product
C2244.3820;, CONELOG Titanium Base CC ¿3.8GH2.0 inkl HS Product Usage: Endosseous dental implant abutment CONELOG Abutments are intended to be used to fabricate prosthetic restorations in conjunction with CONELOG implants to support prostheses in the maxillary and/or mandibul
Category
Medical Device
Distribution
4 states
ModerateFDA (Devices)·Z-2212-2013·2013-09-25
Zeppessis Reprocessed Manifolds Recalled for Lack of FDA Clearance
Zeppessis Reprocessing is recalling reprocessed single-use manifolds for Stryker Neptune systems because they lack FDA 510(k) clearance and a validated cleaning protocol.
Product
Zeppessis' reprocessed single-use manifolds (filters) for the Stryker Neptune 1 and Neptune 2 Waste Management Systems: The Neptune Waste management system is intended to be used in the Operating Room, Surgical Centers and Doctor's Offices to collect and dispose of surgical fl
Category
Medical Device
Distribution
4 states
ModerateFDA (Devices)·Z-2107-2013·2013-09-04
SpineNet Bone Marrow Aspiration Needle Kit Recalled for Lack of FDA Clearance
SpineNet is recalling 100 units of Bone Marrow Aspiration Needle Kits because they were marketed for use with the SpineNet ACC device without FDA clearance or approval.
Product
SpineNet Bone Marrow Aspiration Needle Kit (which is the Ranfac Bone Marrow Aspiration Needle #74150-01M). Use to aspirate bone morrow.
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1363-2013·2013-05-29
Progressive Medical Recalls PTFE Coated Laparoscopic Electrosurgical Electrodes
Progressive Medical Inc. is recalling PTFE Coated Disposable Electrosurgical Electrodes because the product coatings require 510K approval.
Product
Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Laparoscopic Electrode PTFE Coated J- Hook 44cm Length, Product number P0021X Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes used in Elect
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1353-2013·2013-05-29
Progressive Medical Recalls PTFE Coated Disposable Electrosurgical Electrodes
Progressive Medical Inc. is recalling PTFE Coated Disposable Electrosurgical Electrodes because product coatings require 510K approval.
Product
Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Laparoscopic Electrode PTFE Coated L Hook 44cm Length, Product number P0020X Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes used in Electros
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1361-2013·2013-05-29
Progressive Medical Recalls PTFE Coated Disposable Electrosurgical Electrodes
Progressive Medical Inc. is recalling PTFE Coated Disposable Electrosurgical Electrodes because product coatings require 510K approval.
Product
Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - NON-STICK CAUTERY TIP PTFE Coated Needle 2.75" (6.99cm) Length, Product number P0013 Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes used i
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1355-2013·2013-05-29
Progressive Medical Recalls PTFE Coated Laparoscopic Electrodes
Progressive Medical is recalling PTFE coated laparoscopic electrodes because the product coatings require 510K approval.
Product
Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -Laparoscopic Electrode PTFE Coated Curved Blade 33cm Length, Product number P0019 Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes used in El
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1350-2013·2013-05-29
Progressive Medical Recalls PTFE Coated Disposable Electrosurgical Electrodes
Progressive Medical is recalling PTFE Coated Disposable Electrosurgical Electrodes because the product coatings require 510K approval.
Product
Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Laparoscopic Electrode PTFE Coated L Hook 33cm Length, Product number P0020, Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes used in Electr
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1356-2013·2013-05-29
Progressive Medical Recalls PTFE Coated Disposable Electrosurgical Electrodes
Progressive Medical is recalling PTFE coated disposable electrosurgical electrodes because product coatings require 510K approval.
Product
Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -NON-STICK CAUTERY TIP PTFE Modified Coated Blade 6.5" (16.51cm) Length, Product number P0014M Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrode
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1362-2013·2013-05-29
Progressive Medical Recalls PTFE Coated Electrosurgical Electrodes
Progressive Medical is recalling PTFE coated disposable electrosurgical electrodes because the product coatings require 510K approval.
Product
Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - NON-STICK CAUTERY TIP PTFE Coated Sharp Needle 2.00" (5.08cm) Length, Product number P0118 Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes u
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1358-2013·2013-05-29
Progressive Medical Recalls PTFE Coated Electrosurgical Electrodes
Progressive Medical is recalling PTFE coated disposable electrosurgical electrodes because the product coatings require 510K approval.
Product
Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Laparoscopic Electrode PTFE Coated Wire L Hook 44cm Length, Product number P0100X Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes used in E
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1357-2013·2013-05-29
Progressive Medical Recalls PTFE Coated Laparoscopic Electrosurgical Electrodes
Progressive Medical is recalling PTFE Coated Disposable Electrosurgical Electrodes because the product coatings require 510K approval.
Product
Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Laparoscopic Electrode PTFE Coated Spatula 33cm Length, Product number P0018 Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes used in Electr
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1351-2013·2013-05-29
Progressive Medical Recalls PTFE Coated Disposable Electrosurgical Electrodes
Progressive Medical Inc is recalling PTFE Coated Disposable Electrosurgical Electrodes because the product coatings require 510K approval.
Product
Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - NON-STICK CAUTERY TIP PTFE Coated Blade 2.50" (6.40) Length, Product number P0012, Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes used in
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1354-2013·2013-05-29
Progressive Medical Recalls PTFE Coated Disposable Electrosurgical Electrodes
Progressive Medical Inc. is recalling PTFE Coated Disposable Electrosurgical Electrodes because the product coatings require 510K approval.
Product
Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - NON-STICK CAUTERY TIP PTFE Modified Coated Blade 2.50" (6.40cm) Length, Product number P0012M Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrod
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1364-2013·2013-05-29
Progressive Medical Recalls PTFE Coated Disposable Electrosurgical Electrodes
Progressive Medical is recalling PTFE Coated Disposable Electrosurgical Electrodes because the product coatings require 510K approval.
Product
Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Push Button Pencil With PTFE Blade and Holster, Product number P0035H Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Rx Only Electrodes used in Electrosurgeries
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1348-2013·2013-05-29
Progressive Medical Recalls PTFE Coated Disposable Electrosurgical Electrodes
Progressive Medical Inc. is recalling PTFE Coated Disposable Electrosurgical Electrodes because the product coatings require 510K approval.
Product
Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - NON-STICK CAUTERY TIP PTFE Modified Coated Needle 2.75" (6.99cm) Length, Product number P0013M, Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electr
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1359-2013·2013-05-29
Progressive Medical Recalls PTFE Coated Disposable Electrosurgical Electrodes
Progressive Medical Inc. is recalling PTFE Coated Disposable Electrosurgical Electrodes because the product coatings require 510K approval.
Product
Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Laparoscopic Electrode PTFE Coated Wire L Hook Split 33cm Length,Product number P0020S Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes use
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1349-2013·2013-05-29
Progressive Medical Recalls PTFE Coated Electrosurgical Electrodes
Progressive Medical is recalling PTFE Coated Disposable Electrosurgical Electrodes because the product coatings require 510K approval.
Product
Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - NON-STICK CAUTERY TIP PTFE Coated Blade 6.5" (16.51cm) Length, Product number P0014, Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes used i
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1352-2013·2013-05-29
Progressive Medical Recalls PTFE Coated Electrosurgical Electrodes
Progressive Medical Inc. is recalling PTFE coated disposable electrosurgical electrodes because the product coatings require 510K approval.
Product
Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Laparoscopic Electrode PTFE Coated Wire L Hook 33cm Length, Product number P0100 Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes used in Elec
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1360-2013·2013-05-29
Progressive Medical Recalls PTFE Coated Laparoscopic Electrosurgical Electrodes
Progressive Medical is recalling PTFE coated laparoscopic electrosurgical electrodes because the product coatings require 510K approval.
Product
Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Laparoscopic Electrode PTFE Coated J Hook 33cm Length, Product number P0021, Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes used in Elect
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1080-2013·2013-05-01
Stellate Systems Recalls Harmonie Software Due to FDA Clearance Issues
Stellate Systems is recalling Harmonie software versions 5.1 to 6.2e because the product's labeling indications have not been cleared by the FDA for sale in the USA.
Product
Harmonie software versions 5.1 uo to 6.2e : Harmonie-E Long Term Monitoring system (Models HSYS-REC-WD, HSYS-REC-WT; HSYS-REC0LT2; HSYS-REC-EAMP) Product in use with Harmonie-E Long Term Monitoring System : ICTA-S & ICTA-D Seizure Detector, Slow wave Seizure Detector Harmonie
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0902-2013·2013-03-13
Salyer Prn Biomedical Recalls Century Console Base Units
Salyer Prn Biomedical is recalling 9 Century Console Base units because the addition of a UPS Battery Backup did not comply with FDA premarket notification regulations.
Product
Century Console Base, Model #043625051b. Intended for use as a platform for other ancillary equipment and disposable products in cardiopulmonary surgical procedures.
Category
Medical Device
Distribution
3 states
ModerateFDA (Devices)·Z-0761-2013·2013-03-06
GE Healthcare Recalls Brivo XR385 X-Ray Systems Due to Software Issue
GE Healthcare is recalling nine Brivo XR385 X-Ray systems in the US due to a software issue affecting visual indications required by regulations.
Product
GE Healthcare Brivo XR385 DR-F/ X-Ray System X-Ray System
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0873-2013·2013-03-06
KY Sensitive Jelly Personal Lubricant Recalled for Lack of FDA Clearance
McNeil-PPC Inc. is recalling KY Sensitive Jelly Personal Lubricant because the product is not cleared for marketing in the US.
Product
KY SENSITIVE TM JELLY Personal Lubricant. The product is packaged into 3 oz tubes, which are then packed into a printed carton. Distributed by McNeil-PPC Inc.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0874-2013·2013-03-06
KY SilkE Vaginal Moisturizer Recalled for Lack of FDA Clearance
McNeil-PPC is recalling KY SilkE Vaginal Moisturizer because the product is not cleared for marketing in the US.
Product
KY SilkE Vaginal Moisturizer and Personal Lubricant. The product is packaged in 2.5 oz bottles, which are then packed into a printed carton. Distributed by McNeil-PPC Inc.
Category
Medical Device
Distribution
Distributed nationwide