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.

526–536 of 536

HighFDA (Devices)·Z-0654-2013·2013-02-20
Lockheed Martin Gyrocam Systems Recalled for Laser Safety Non-Compliance
Lockheed Martin Gyrocam Systems are being recalled because they contain Class IIIb lasers that failed FDA performance standards and were sold without a required variance.
Product
Lockheed Martin Gyrocam Systems ( LMGS) LMGS 15" camera systems. Laser pointer and illuminator used for law enforcement surveillance from aircraft. Models DNV, TS and DS
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0702-2013·2013-02-06
Philips Juno DRF X-ray System Recalled for Display Compliance Issues
Philips Healthcare is recalling 16 Juno DRF X-ray systems because fluoroscopy dose values may not display correctly at the operator's position.
Product
Juno DRF , X-ray system, diagnostic, Fluoroscopic, general-purpose Model: 70920 Product Usage: Universal R/F, general use
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0615-2013·2013-01-02
Arjo Flowtron Trio DVT Pump Recalled for Lack of FDA Approval
Arjo, Inc. is recalling 2,859 Flowtron Trio DVT Pumps because they were marketed without proper FDA approval.
Product
Flowtron Trio DVT Pump; an Rx intermittent pneumatic compression deep vein thrombosis pump; ArjoHuntleigh AB, Eslov, Sweden; Model 512003; a non-invasive prophylaxis system for reducing the incidence of deep vein thrombosis.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0263-2013·2012-11-14
Shimadzu Recalls Mobile X-ray Systems for Beam Quality Non-Compliance
Shimadzu Medical Systems is recalling 133 mobile X-ray systems because certain units may not meet federal beam quality standards.
Product
0.7/1.3U163CS-36 In combination with below systems MobileArt Evolution, MobileDaRt Evolution Product Usage: The device is a mobile X-ray system in order to take general radiography of patients in the hospital who cannot move and/or of outpatients in emergency.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0264-2013·2012-11-14
Shimadzu Recalls Mobile X-ray Systems for Beam Quality Non-Compliance
Shimadzu Medical Systems is recalling 5 mobile X-ray systems because they may not meet federal beam quality standards.
Product
0.7/1.2JG326D-265 Product Usage: The device is a mobile X-ray system in order to take general radiography of patients in the hospital who cannot move and/or of outpatients in emergency.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0262-2013·2012-11-14
Shimadzu Recalls Mobile X-ray Systems for Beam Quality Non-Compliance
Shimadzu is recalling 288 mobile X-ray systems and related components because they may not meet federal standards for beam quality.
Product
0.7U163CS-36 In combination with below systems MUX-100H, MUX-100D, MobileArt Evolution Brand Name: MUX-100H. Classification Name: Mobile x-ray system. Device Model#MUX-100H. Product Usage: The device is a mobile X-ray system in order to take general radiography of
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2467-2012·2012-10-03
K-Y Liquibeads Vaginal Moisturizer Recalled for Regulatory Compliance
Johnson & Johnson is voluntarily recalling K-Y Liquibeads Vaginal Moisturizer to address FDA concerns regarding the product's medical device clearance status.
Product
KY LIQUIBEADS Vaginal Moisturizer; Distributed By: McNeil-PPC, Inc. Skillman, NJ 08558-9418; UPC 380041087704; 380040087958. Personal lubricant
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2217-2012·2012-08-22
DePuy Orthopaedics Recalls Unimplanted Custom Implant Devices
DePuy Orthopaedics is retrieving 8,338 custom implant devices that were ordered but not implanted, following an FDA Warning Letter.
Product
DePuy Custom Implant Devices Packaging: Packaging was not standardized on customs, it was dependant on the geometry of the product Product Usage: Description: Devices meeting the regulatory definition of a custom medical device are those which are provided by prescriptio
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2183-2012·2012-08-22
Beauty Angel Device Recalled for Lack of FDA Clearance
JK Products & Services is recalling Beauty Angel devices because they were marketed without the required FDA 510(k) clearance.
Product
BeautyAngel Health Fitness Natural Collagen Stimulation Anti Aging For human use.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2029-2012·2012-07-25
Gulf Fiberoptics Recalls GMF-RC65 Surgical Headlight Cables
Gulf Fiberoptics, Inc. is recalling 169 GMF-RC65 Replacement Surgical Headlight Cables because the light-transmitting fiber material differs from the approved 510(k) design.
Product
GMF-RC65 Replacement Surgical Headlight Cable for Cogent Microlink. GMF-RC65 Replacement Surgical Headlight Cable for Cogent Microlink is used to transmit light.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1713-2012·2012-07-11
Frozen Korean Oysters Recalled Due to Shipper Certification Issues
Seoul Shik Poom, Inc. is recalling 412 cases of frozen oysters because the shippers were delisted from the FDA's International Certification System.
Product
Frozen Oysters, Net Wt 1 LBS (454g). Distributed by: Seoul Shik Poom, Engleside, NJ. Origin: Republic of Korea.
Category
Food
Distribution
Distributed nationwide