Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

32451–32475 of 40449

ModerateFDA (Devices)·Z-2278-2015·2015-08-05
Hardy Diagnostics Recalls Multiple Microbiology Media Due to Lack of Clearance
Hardy Diagnostics is recalling several microbiology media products, including BEA Broth with Vancomycin, because they lack FDA 510(k) clearance.
Product
Hardy Diagnostics BEA Broth with Vancomycin container type: 13x100mm tube packaged: 20 tubes/box fill: 2ml Product Usage: BEA (Bile Esculin Azide) Broth with Vancomycin is for the surveillance of vancomycin resistant enterococci (VRE) not to be used for susceptibility…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2290-2015·2015-08-05
Anspach Fluted Ball Dissection Tools Recalled for Labeling Inconsistency
The Anspach Effort, Inc. is recalling 353 Fluted Ball dissection tools because the labeled shaft exposure may be inconsistent with actual usage.
Product
ANSPACH - Fluted Ball; 9MM REF L-9B-G1 Cutting shaping bone including spine and cranium.
Category
Medical Device
Distribution
17 states
ModerateFDA (Devices)·Z-2297-2015·2015-08-05
Anspach G1 Dissection Tools Recalled for Inconsistent Shaft Exposure Labeling
The Anspach Effort, Inc. is recalling 95 G1 dissection tools because the labeled shaft exposure may not be consistent with all listed attachments, potentially resulting in greater exposure than specified.
Product
ANSPACH - 6MM x 11.3MM Fluted Barrel; REF M-6BA-A-G1 Cutting shaping bone including spine and cranium.
Category
Medical Device
Distribution
17 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-2312-2015·2015-08-05
Anspach G1 Dissection Tools Recalled for Inconsistent Shaft Exposure Labeling
The Anspach Effort, Inc. is recalling 78 G1 dissection tools because the specified shaft exposure may be greater than labeled when used with certain attachments.
Product
ANSPACH - 2.3MM Fluted Matchstick, Extends 22MM; REF S-8N-L-G1 Cutting shaping bone including spine and cranium.
Category
Medical Device
Distribution
17 states
ModerateFDA (Devices)·Z-2244-2015·2015-08-05
EXP Pharmaceutical Services Recalls SECURESTRAP Absorbable Strap Fixation Devices
EXP Pharmaceutical Services Corp is recalling SECURESTRAP 5mm Absorbable Strap Fixation Devices because the company failed to register as a medical device establishment or maintain its own quality system.
Product
Medical Device Exchange SECURESTRAP 5mm Absorbable Strap Fixation Device; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number STRAP25; EXP (repackager), Ethicon (OEM) Strap, implantable.
Category
Medical Device
Distribution
6 states
ModerateFDA (Devices)·Z-2294-2015·2015-08-05
Anspach G1 Dissection Tools Recalled for Inconsistent Shaft Exposure Labeling
The Anspach Effort, Inc. is recalling 92 G1 dissection tools because the labeled shaft exposure may be inconsistent with actual use, potentially resulting in greater exposure.
Product
ANSPACH - 4MM x 11 MM Fluted Barrel, 14 Flutes; REF M-4BA-A-G1. Cutting shaping bone including spine and cranium.
Category
Medical Device
Distribution
17 states
ModerateFDA (Devices)·Z-2242-2015·2015-08-05
EXP Recalls PhysioMesh Surgical Mesh Due to Regulatory Non-Compliance
EXP Pharmaceutical Services Corp is recalling two units of PhysioMesh surgical mesh because the company failed to register as a medical device establishment or maintain its own quality system.
Product
Medical Device Exchange PhysioMesh Flexible Composite Mesh 10cm x 15cm; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number PHY1015V; EXP (repackager), Ethicon (OEM) Mesh, surgical, polymeric
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-2280-2015·2015-08-05
Anspach Fluted Drum Dissection Tools Recalled for Inconsistent Shaft Exposure
The Anspach Effort, Inc. is recalling 65 Fluted Drum dissection tools because the specified shaft exposure may be inconsistent with attachments, potentially resulting in greater exposure.
Product
ANSPACH - Fluted Drum, Side Cut only 10MM x 14MM , REF L-10DRC-G1 Cutting shaping bone including spine and cranium.
Category
Medical Device
Distribution
17 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…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2218-2015·2015-08-05
EXP Pharmaceutical Services Recalls Versaport Bladeless Trocar Devices
EXP Pharmaceutical Services Corp is recalling Versaport Bladeless Trocar devices because the company failed to register as a medical device establishment or establish its own quality system.
Product
Medical Device Exchange - Versaport Bladeless Trocar w/ Fixation Cannula 5mm; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number NB5STF; EXP (repackager), Covidien (OEM) Laparoscope, General & Plastic Surgery
Category
Medical Device
Distribution
6 states
ModerateFDA (Devices)·Z-2311-2015·2015-08-05
Anspach G1 Dissection Tools Recalled for Inconsistent Shaft Exposure Labeling
The Anspach Effort, Inc. is recalling 80 G1 dissection tools because the labeled shaft exposure may be inconsistent with actual use, potentially resulting in greater exposure than specified.
Product
ANSPACH - 5MM Coarse Diamond Ball, 22MM Shaft Exposure; REF S-5DC-22-G1 Cutting shaping bone including spine and cranium.
Category
Medical Device
Distribution
17 states
ModerateFDA (Devices)·Z-2277-2015·2015-08-05
Hardy Diagnostics Recalls Multiple Microbiology Media Due to Lack of 510(k) Clearance
Hardy Diagnostics is recalling several microbiology media products, including BEA Agar with VGA, because they lack FDA 510(k) clearance.
Product
Hardy Diagnostics BEA Agar with VGA container type: 15x100mm monoplate packaged: 10 places/sleeve Product Usage: BEA (Bile Esculin Azide) Agar with Vacomycin, Gentamicin, and Amphotericin B is for the selective isolation of vancomycin resistant enterococci (VRE).
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2272-2015·2015-08-05
Synthes Maxillary Plates Recalled for Incorrect Laser Etch Orientation
Synthes (USA) Products LLC is recalling 31 pre-bent maxillary plates due to potential incorrect laser etch denoting orientation.
Product
Synthes TI Matrix Pre-Bent Maxillary Plate / 2mm ADVMNT/0.8mm THK/L and Synthes TI Matrix Pre-Bent Maxillary Plate / 2mm ADVMNT/0.8mm THK/R. The Synthes Matrix ORTHOGNATHIC Fixation System is intended for use in selective trauma of the midface and craniofacial skeleton…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2230-2015·2015-08-05
EXP Recalls Fiberwire Suture Scissors Due to Registration Violations
EXP Pharmaceutical Services Corp is recalling Fiberwire Suture Scissors because the company failed to register as a medical device establishment or establish its own quality system.
Product
Medical Device Exchange FIBERWIRE SUTURE SCISSOR; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number AR-11796; EXP (repackager), Arrow (OEM) Electrosurgical, cutting & coagulation & accessories.
Category
Medical Device
Distribution
6 states
ModerateFDA (Devices)·Z-2299-2015·2015-08-05
Anspach 7MM Fluted Acorn Dissection Tools Recalled for Labeling Inconsistency
The Anspach Effort, Inc. is recalling 189 Anspach 7MM Fluted Acorn dissection tools because the specified shaft exposure on the label may not be consistent with all listed attachments.
Product
ANSPACH - 7MM Fluted Acorn; REF M-7AC-G1 Cutting shaping bone including spine and cranium.
Category
Medical Device
Distribution
17 states
ModerateFDA (Devices)·Z-2234-2015·2015-08-05
EXP Pharmaceutical Services Recalls Unregistered Transcatheter Septal Occluders
EXP Pharmaceutical Services Corp is recalling 12mm vascular transcatheter septal occluders because the company failed to register as a medical device establishment or establish a quality system.
Product
Medical Device Exchange 12MM VASCULAR; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number 9-AVP2-012; EXP (repackager), Aga Medical (OEM) Transcatheter septal occluder
Category
Medical Device
Distribution
6 states
ModerateFDA (Devices)·Z-2287-2015·2015-08-05
Anspach Fluted Barrel Dissection Tools Recalled for Labeling Inconsistency
The Anspach Effort, Inc. is recalling 110 fluted barrel dissection tools because the labeled shaft exposure may be inconsistent with actual usage.
Product
ANSPACH - Fluted Barrel; 8MM x 12.5MM REF L-8BA-G1 Cutting shaping bone including spine and cranium.
Category
Medical Device
Distribution
17 states
ModerateFDA (Devices)·Z-2265-2015·2015-08-05
Ivoclar Vivadent Recalls IPS Empress Universal Glaze Spray Due to Coarse Particles
Ivoclar Vivadent is recalling IPS Empress Universal Glaze Spray because complaints indicated coarse particles in the glazed surface of dental restorations.
Product
IPS Empress Universal Glaze Spray 270 mL, Product Code/Model/Catalog Number 609432AN, Rx only. Porcelain glaze spray used in the fabrication of dental restorations
Category
Medical Device
Distribution
4 states
ModerateFDA (Devices)·Z-2219-2015·2015-08-05
EXP Pharmaceutical Services Recalls Unregistered Implantable Staple Loading Units
EXP Pharmaceutical Services Corp is recalling three units of implantable staple loading units because the company failed to register as a medical device establishment or maintain a quality system.
Product
Medical Device Exchange - Loading Unit w/ DST Series Technology 60mm - 3.5mm; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number TA6035L; EXP (repackager), Covidien (OEM) Implantable Staple
Category
Medical Device
Distribution
6 states
ModerateFDA (Devices)·Z-2263-2015·2015-08-05
McKesson Paragon Laboratory Management Software Recall for Data Display Errors
McKesson Technologies is recalling Paragon Laboratory Management software versions 12.1 and 12.1.1 because the Final Cumulative Report may display incorrect data when used with Microsoft SQL Server 2012.
Product
Paragon Laboratory Management
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2303-2015·2015-08-05
Anspach G1 Dissection Tools Recalled for Inconsistent Shaft Exposure Labeling
The Anspach Effort, Inc. is recalling 118 G1 dissection tools because the specified shaft exposure on the label may not be consistent with all listed attachments.
Product
ANSPACH - 5MM Fluted Ball, Extends 27MM; REF M-5B-27-G1. Cutting shaping bone including spine and cranium.
Category
Medical Device
Distribution
17 states
ModerateFDA (Devices)·Z-2210-2015·2015-08-05
MTF Recalls Allograft Cortical Pins Due to Diameter Labeling Error
Musculoskeletal Transplant Foundation is recalling one lot of Allograft Cortical Pins because the 2.0 mm label may contain 2.4 mm pins.
Product
Cortical Pin 2.0 mm,Sterile, FREEZE DRIED: Store at ambient temperature. Do Not freeze.
Category
Medical Device
Distribution
7 states
ModerateFDA (Devices)·Z-2223-2015·2015-08-05
EXP Pharmaceutical Services Recalls Unregistered Medical Suction Devices
EXP Pharmaceutical Services Corp is recalling sterile suction devices because the company failed to register as a medical device establishment or maintain its own quality system.
Product
Medical Device Exchange - Silicone Round Drain; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number SU130-1321; EXP (repackager), Jackson Pratt (OEM) Apparatus, suction, single patient use, portable, nonpowered
Category
Medical Device
Distribution
6 states

How to read this listing

Filters

32451–32475 of 40449