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.

301–325 of 536

ModerateFDA (Food)·F-0481-2016·2016-01-20
Garden Harvest Recalls Pickled Beets Manufactured Without License
Garden Harvest is recalling Dutch Country Kettles Homemade Pickled Beets because the firm was manufacturing acidified foods without a license.
Product
DUTCH COUNTRY KETTLES HOMEMADE Pickled Beets Ingredients: Beets, Water, Vinegar, Sugar, Salt. Dutch Country Kettles 6732 Pavey Road. Leesburg, OH 45135 1-937-780-6718 1 Pint (1 lb. 3oz) 538g UPC 6 98241 12224 9 & 1 Quart (32 oz) 907g UPC 6 98241 14444 9
Category
Food
Distribution
3 states
ModerateFDA (Food)·F-0477-2016·2016-01-20
Garden Harvest Recalls Bino's Italian Sweet Peppers Due to Unlicensed Manufacturing
Garden Harvest is recalling Bino's Italian Sweet Peppers because the firm was manufacturing acidified foods without a license. The product was shipped to Ohio, Florida, and West Virginia.
Product
BINO'S ITALIAN SWEET PEPPERS Ingredients: Bell peppers, onions, vinegar, garlic, sugar, tomato sauce, tomato puree, salt and olive oil. NET WT 16 oz UPC 8 67752 00012 8 NET WT 32 oz UPC 8 67752 00010 4
Category
Food
Distribution
3 states
ModerateFDA (Food)·F-0491-2016·2016-01-20
Garden Harvest Black Bean Salsa Recalled for Unlicensed Acidified Food Production
Garden Harvest is recalling 41 cases of black bean salsa because the firm was manufacturing acidified foods without a license.
Product
Kiem's Garden Harvest black bean salsa 1 PT (14 oz 397g) Ingredients: beans, corn, tomato***Manufactured by: Keim's Garden Harvest (937) 515-4518 Honeysuckle Lane Wellston, OH UPC 6 09722 32347 5
Category
Food
Distribution
3 states
ModerateFDA (Food)·F-0483-2016·2016-01-20
Garden Harvest Recalls Herbert's Chow-Chow Due to Unlicensed Manufacturing
Garden Harvest is recalling specific lots of Herbert's chow-chow because the firm was manufacturing acidified foods without a license.
Product
HERBERT'S chow-chow Mild New Weight 12.8 oz (363g) Ingredients: Cabbage***Manufactured for: The All-American Relish Company. North Canton OH 44720 330-842-0168 UPC 8 57025 00270 6
Category
Food
Distribution
3 states
ModerateFDA (Food)·F-0482-2016·2016-01-20
Garden Harvest Recalls Herbert's Chow-Chow for Unlicensed Acidified Food Production
Garden Harvest is recalling 156 cases of Herbert's chow-chow because the firm was manufacturing acidified foods without a license.
Product
HERBERT'S chow-chow Hot New Weight 12.8 oz (363g) Ingredients: Cabbage***Manufactured for: The All-American Relish Company. North Canton OH 44720 330-842-0168 UPC 8 57025 00270 6
Category
Food
Distribution
3 states
ModerateFDA (Food)·F-0486-2016·2016-01-20
Garden Harvest Tomato Salsa Recalled for Unlicensed Acidified Food Manufacturing
Garden Harvest is recalling tomato salsa because the firm was manufacturing acidified foods without a license. The product was distributed in Ohio, Florida, and West Virginia.
Product
Keim's Garden Harvest tomato salsa 1 PT (14 oz 397g) Ingredients: tomatoes, onions, peppers, herbs***Manufactured by: Keim's Garden Harvest (937) 515.4518 2232 Honeysuckle Lane Wellston OH 45692 mild UPC 6 09722 32345 1 medium UPC 6 09722 32343 7, hot UPC 6 09722 32344 4
Category
Food
Distribution
3 states
ModerateFDA (Food)·F-0474-2016·2016-01-20
Garden Harvest Recalls Abruzzi's Hot Peppers in Oil for Unlicensed Manufacturing
Garden Harvest is recalling 1,143 cases of Abruzzi's Hot Peppers in Oil because the firm was manufacturing acidified foods without a license.
Product
Abruzzi's Hot Peppers in oil 15 Fl Oz (444 ml) Manufactured For: Abruzzis Hot Peppers, LLC, 371 Marwood Drive, S.E. Warren, Ohio 44484 (330) 883-7933 UPC 8 51071 00500 1
Category
Food
Distribution
3 states
ModerateFDA (Food)·F-0475-2016·2016-01-20
Garden Harvest Recalls Barney's Hot Peppers Due to Unlicensed Manufacturing
Garden Harvest is recalling 106 cases of Barney's Hot Peppers because the firm was manufacturing acidified foods without a license.
Product
Barney's Hot Peppers 16 oz (443 ml) Ingredients: Hot Peppers, Canola Oil, Garlic, Oregano, Salt, Acidic Calcium Sulfate Distributed by: Barney's Hot Peppers 2061 Elm Road Warren, Ohio 44483 330-964-2922 UPC # 7 01807 99994 7
Category
Food
Distribution
3 states
ModerateFDA (Food)·F-0487-2016·2016-01-20
Keim's Garden Harvest Pickled Beets Recalled for Unlicensed Manufacturing
Keim's Garden Harvest pickled beets are being recalled because the manufacturer was producing acidified foods without a required license.
Product
Keim's Garden Harvest pickled beets Ingredients: red beets, water, sugar, vinegar, spices, salt. Manufactured by: Keim's Garden Harvest (937) 515.4518 2232 Honeysuckle Lane Wellston OH 45692 14 oz UPC 6 09722 32336 9, 32 oz UPC 6 09722 32339 0
Category
Food
Distribution
3 states
ModerateFDA (Food)·F-0479-2016·2016-01-20
Garden Harvest Recalls Cleveland Pickle Garlic Dill for Unlicensed Manufacturing
Garden Harvest is recalling 146 cases of Cleveland Pickle Original Garlic Dill because the firm was manufacturing acidified foods without a license.
Product
Cleveland Pickle Original Garlic Dill 16 oz (454 g) Ingredients: Cucumbers, Water***Manufactured For: CLEVELAND PICKLE 850 EUCLID AVE. CLEVELAND OH 44114 216-575-1111 UPC 8 67051 00001 0
Category
Food
Distribution
3 states
ModerateFDA (Food)·F-0495-2016·2016-01-20
Garden Harvest Recalls Patty's Peppers for Unlicensed Acidified Food Manufacturing
Garden Harvest is recalling Patty's Peppers Hungarian Hot & Sweet Peppers because the firm was manufacturing acidified foods without a license.
Product
PATTY'S PEPPERS HUNGARIAN HOT & SWEET PEPPERS Uncle Joe's Original Recipe NET WT 16 oz & 32 oz Ingredients: Hungarian Hot Wax Peppers, Garlic, Vinegar, All Natural Ketchup, Sugar, Canola Oil, pattyspeppers.com UPC 7 48252 07486 7
Category
Food
Distribution
3 states
ModerateFDA (Food)·F-0484-2016·2016-01-20
Garden Harvest Recalls Herbert's Chow-Chow Due to Unlicensed Acidified Food Production
Garden Harvest is recalling Herbert's chow-chow because the firm was manufacturing acidified foods without a license. The product was distributed to Ohio, Florida, and West Virginia.
Product
HERBERT'S chow-chow Original New Weight 12.8 oz (363g) Ingredients: Cabbage***Manufactured for: The All-American Relish Company. North Canton OH 44720 330-842-0168 UPC 8 57025 00270 6
Category
Food
Distribution
3 states
ModerateFDA (Food)·F-0470-2016·2016-01-20
Garden Harvest Recalls Heiney Hot Salsa for Unlicensed Acidified Food Production
Garden Harvest is recalling 26 cases of Heiney Hot Salsa because the firm was manufacturing acidified foods without a license.
Product
A BIT OF A BITE SALSA HEINEY HOT SALSA NET WT. 128 OZ INGREDIENTS: DICED TOMATOES***FRESH ZUCCHINI, FRESH ONIONS***FRESH JALAPENO PEPPERS***FRESH HABANERO PEPPERS. A Bit of Bite Salsa 1243 Nouvelle Drive Miamisburg, OH 45342 UPC 6 42125 95415 0
Category
Food
Distribution
3 states
ModerateFDA (Devices)·Z-0556-2016·2016-01-06
Biomerieux Recalls Granada Biphasic Broth Due to Missing FDA Clearance
Biomerieux Inc is recalling 24 cartons of Granada Biphasic Broth because the product lacks required FDA 510(k) clearance for marketing in the United States.
Product
Granada Biphasic Broth The product is a selective medium for the screening and identification of Streptococcus agalactiae in pregnant women using clinical specimens.
Category
Medical Device
Distribution
9 states
HighFDA (Devices)·Z-0281-2016·2015-11-25
Stryker Recalls PCA Acetabular Inserts Due to Regulatory Omission
Stryker Howmedica Osteonics Corp. is recalling six PCA 10 Degree Hooded Acetabular Inserts because the 22 mm size was inadvertently omitted from the FDA 510(k) clearance.
Product
Stryker PCA 10 Degree Hooded Acetabular Insert ID 22mm, Part of the Howmedica PCA Total Hip System intended for use during total hip arthroplasty. The acetabular insert is used in conjunction with PCA Acetabular Shells and Femoral Heads to restore hip joint biomechanics.
Category
Medical Device
Distribution
1 state
LowFDA (Devices)·Z-0270-2016·2015-11-18
Stryker Spine Recalls Radius Rod to Rod Connectors for Missing Clearance
Stryker Spine is recalling 42 units of Radius Rod to Rod Connectors because the device lacks the required FDA 510(k) clearance.
Product
Stryker Radius 5.5 to 3.5 Rod to Red Connector, REF 48664530. Intended to provide additional support during fusion using autograft or allograft in skeletally mature patients.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0028-2016·2015-10-28
Wismettac Asian Food Recalls Seasoned Beanthread Salad for Regulatory Filing Issues
Wismettac Asian Food is recalling Seasoned Beanthread Salad (Chuka Zensai) due to a lack of required acidified food filing and registration.
Product
Seasoned Beanthread Salad (CHUKA ZENSAI), net wt. 2.2 lbs (1kg), Item No. 82021. Chinese style appetizer labeled as SEASONED BEANTHREAD SALAD (CHUKA ZENSAI) packed in 1 kg clear plastic bags and placed in cardboard cartons containing twelve (12) bags per carton. The bags of
Category
Food
Distribution
1 state
ModerateFDA (Devices)·Z-2740-2015·2015-09-16
DermaPen Pro Micro Needling System Recalled for Lack of FDA Clearance
Derma Pen, LLC is recalling DermaPen Pro Micro Needling Systems because the devices were distributed without FDA clearance or approval.
Product
DermaPen Pro Model, Micro Needling System, a motorized AC powered surgical instrument for dermabrasive use. Each motorized handpiece is packaged within a small box. Each disposable needle cartridge is packaged individually and then placed into boxes of 30 quantities per box.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2320-2015·2015-08-19
GE Laser Centering Device Recalled for Regulatory Non-Compliance
GE Inspection Technologies is recalling 25 laser centering devices for X-ray generators due to potential failure to comply with federal regulations.
Product
GE Optional Laser Centering Device X-ray generator.
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-2245-2015·2015-08-05
EXP Pharmaceutical Services Recalls TAUT Intraducer Peritoneal Catheters
EXP Pharmaceutical Services Corp is recalling TAUT Intraducer Peritoneal Catheters because the company failed to register as a medical device establishment or maintain its own quality system.
Product
Medical Device Exchange TAUT Intraducer Peritoneal Catheter 2mm x 1.6mm x 7.6cm; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number PI-63; EXP (repackager), Teleflex (OEM) Catheter, biliary, surgical
Category
Medical Device
Distribution
6 states
ModerateFDA (Devices)·Z-2246-2015·2015-08-05
EXP Recalls 3.5mm Threaded Cerclage Pins Due to Registration Failures
EXP Pharmaceutical Services Corp is recalling 3.5mm Threaded Cerclage Pins because the company failed to register as a medical device establishment or establish a quality system.
Product
Medical Device Exchange 3.5mm Threaded Cerclage Pin; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number 298.838S; EXP (repackager), Synthes (OEM) Cerclage, fixation
Category
Medical Device
Distribution
6 states
ModerateFDA (Devices)·Z-2215-2015·2015-08-05
EXP Pharmaceutical Services Recalls Unregistered Medical Device Repackaging
EXP Pharmaceutical Services Corp is recalling four units of Trocar VersaPort Plus V2 devices because the company failed to register as a medical device establishment or maintain its own quality system.
Product
Medical Device Exchange - Trocar VersaPort Plus V2; 5mm -11mm; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number 179095P; EXP (repackager), Auto Suture (OEM) Laparoscope, General and Plastic Surgery
Category
Medical Device
Distribution
6 states
ModerateFDA (Devices)·Z-2252-2015·2015-08-05
EXP Pharmaceutical Services Recalls Tracheal Stent Sizing Devices
EXP Pharmaceutical Services Corp is recalling two units of tracheal stent sizing devices due to regulatory non-compliance regarding establishment registration and quality systems.
Product
Medical Device Exchange Aerosizer Stent Sizing Device; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number 90129-501. EXP (repackager), Merit Medical (OEM) Prosthesis, tracheal, expandable
Category
Medical Device
Distribution
6 states
ModerateFDA (Devices)·Z-2249-2015·2015-08-05
EXP Pharmaceutical Services Recalls Unregistered Airway Stent Systems
EXP Pharmaceutical Services Corp is recalling 10x40 Airway Stent Systems because the company failed to register as a medical device establishment or maintain its own quality system.
Product
Medical Device Exchange 10x40 Airway Stent System; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number 90129-209; EXP (repackager), Aero (OEM) Prosthesis, tracheal, expandable
Category
Medical Device
Distribution
6 states
ModerateFDA (Devices)·Z-2273-2015·2015-08-05
Hardy Diagnostics Recalls MacConkey Agar and Other Media for Lack of Clearance
Hardy Diagnostics is recalling specific lots of MacConkey Agar and other diagnostic media because they lack FDA 510(k) clearance.
Product
Hardy Diagnostics MacConkey Agar with CiPRP, 1ug/ml Container type: 15x100mm monoplate packaged: 10 plates/sleeve Product Usage: MacConkey Agar with Ciprofloxacin is used as a screening medium for the selective isolation of Ciprofloxacin-resistant E. coli from clinical s
Category
Medical Device
Distribution
Distributed nationwide