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

25751–25775 of 27722

HighFDA (Devices)·Z-0457-2014·2013-12-18
Hospira Recalls Receptal Canisters Due to Suction Failure
Hospira is recalling 1L Receptal Canisters because the canister and liner may not seat properly, preventing the creation of necessary suction.
Product
Product is labeled in part: LIST NO. 43449; RECEPTAL CANISTER; DO NOT FILL 900 ABOVE THIS LINE; Product of China; Hospira, Inc.,; Lake Forest, IL 60045 USA. Used to isolate suction waste during surgeries, or to clear patient airways, throat or wounds to allow treatment.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0460-2014·2013-12-18
Zimmer NexGen Porous Patella Drill Guide Recall Expansion
Zimmer, Inc. is expanding a recall of NexGen Porous Patella Drill Guides to prevent inadvertent use during surgery, which could cause delays.
Product
NexGen Complete Knee Solution Porous Patella Drill Guide-29mm dia./10mm thickness Non sterile, Rx Only Devices are used in total knee arthroplasty and indicated for patients with severe pain and disability due to conditions such as arthritis, collagen disorders…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0464-2014·2013-12-18
Centurion Sterile Rubber Bands Recalled for Contradictory Latex Labeling
Centurion Medical Products is recalling sterile rubber bands that are labeled as both latex-free and containing natural rubber latex, posing a risk to users with latex allergies.
Product
Centurion Sterile # 84 Rubber Bands Reorder EB84, Caution: This product contains natural rubber latex which may cause allergic reactions. LATEX FREE , CAUTION: FEDERAL lAW (USA) RESTRICTS THIS DEVICE TO SALE BY OR ON THE ORDER OF A PHYSICIAN Single Use Only bands items…
Category
Medical Device
Distribution
3 states
HighFDA (Devices)·Z-0479-2014·2013-12-18
Aesculap GNI161 Bipolar Foot Control Recalled for Energy Failure
Aesculap, Inc. is recalling 85 GNI161 Bipolar Foot Controls because the bipolar energy did not stop after the foot control was released.
Product
Aesculap GNI161 Bipolar Foot Control Product Usage: The Aesculap Bipolar Coagulator is intended for use in surgery to generate electrical power for bipolar instruments. Bipolar coagulators are used in neurosurgery, ENT surgery, urology, laparoscopy, and plastic surgery.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0461-2014·2013-12-18
Zimmer NexGen Knee Implant Components Recalled for Surgical Delay Risk
Zimmer, Inc. is recalling 638 NexGen Complete Knee Solution provisional articular surface devices. The recall is an expansion of a previous action to prevent inadvertent use of associated instruments.
Product
NexGen Complete Knee Solution CR Articular Surface Provisional-Purple 9mm Height Nonsterile Devices are used in total knee arthroplasty and indicated for patients with severe pain and disability due to conditions such as arthritis, collagen disorders, post-traumatic loss of…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0459-2014·2013-12-18
Zimmer NexGen Porous Patella Drill Guide Recall Expansion
Zimmer, Inc. is expanding a recall of NexGen Porous Patella Drill Guides to include five additional instruments. These devices may be inadvertently used during surgery, causing delays.
Product
NexGen Complete Knee Solution Porous Patella Drill Guide-26mm dia./10mm thickness Non sterile, Rx Only Devices are used in total knee arthroplasty and indicated for patients with severe pain and disability due to conditions such as arthritis, collagen disorders…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0478-2014·2013-12-18
Steris Recalls AMSCO Evolution Steam Sterilizer Transfer Carriages
Steris Corporation is recalling 936 AMSCO Evolution steam sterilizer transfer carriages because they may unlatch when overloaded or maneuvered with excessive force.
Product
AMSCO¿ Evolution¿ steam sterilizer Transfer Carriage. Product Usage: Mobile, wheeled transportation unit utilized to carry, load, & unload the Loading Car into and out of steam sterilizer units.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0463-2014·2013-12-18
Zimmer NexGen Knee Instruments Recalled Due to Potential Surgical Delay
Zimmer, Inc. is recalling five NexGen Micro knee instruments because they may be used incorrectly, causing surgical delays.
Product
NexGen Complete Knee Solution CR Articular Surface Provisional-Striped Green 9mm Height Nonsterile Devices are used in total knee arthroplasty and indicated for patients with severe pain and disability due to conditions such as arthritis, collagen disorders, post-traumatic…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0480-2014·2013-12-18
Zimmer Recalls NexGen Knee Components Due to Stem Locking Failure
Zimmer, Inc. is recalling 128 NexGen Complete Knee Solutions Stemmed Tibial Components because the stem may not lock into the tibia.
Product
NexGen¿ Complete Knee Solutions Stemmed Tibial Component Precoat NexGen Tibial Baseplates are part of the NexGen systems of semi-constrained, non-linked condylar knee prosthesis. The device is indicated for patients with severe knee pain and disability due to: Rheumatoid…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0438-2014·2013-12-11
Siemens ARTISTE Linear Accelerator Recall for Dark Current Radiation Risk
Siemens is recalling 26 ARTISTE Linear Accelerator systems due to a potential dark current radiation risk during specific IMRT treatments.
Product
SIEMENS brand ARTISTE Linear Accelerator Linac systems with component: any photon unflat beam option (Multiple X feature) in combination with the IMRT or mARC option. A family of linear accelerator systems is to deliver X-ray photon and electron radiation for the therapeutic…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0437-2014·2013-12-11
Siemens Oncor Linear Accelerators Recalled for Dark Current Radiation Risk
Siemens is recalling three Oncor Linear Accelerator units due to a potential dark current radiation risk during specific IMRT treatments.
Product
SIEMENS brand ONCOR series Linear Accelerator Linac systems with component: any photon unflat beam option(Multiple X feature) in combination with the IMRT or mARC option. A family of linear accelerator systems is to deliver X-ray photon and electron radiation for the…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0452-2014·2013-12-11
Synthes Recalls Titanium Trochanteric Fixation Nail Systems Due to Missing Bend
Synthes USA is recalling 17 units of the Titanium Trochanteric Fixation Nail (TFN) System because two lots are missing a required second bend in the nail.
Product
Titanium Trochanteric Fixation Nail (TFN)System Intended to treat stable and unstable fractures of the proximal femur.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0451-2014·2013-12-11
Abbott i-STAT PT/INR Cartridges Recalled for Potential INR Errors
Abbott Point of Care Inc. is recalling i-STAT PT/INR cartridges because they may display incorrectly elevated INR results.
Product
Abbott i-STAT PT/INR cartridges Abbott Point of Care Inc., Princeton, NJ 08540 The i-Stat PT a prothrombin time test is useful for monitoring patients receiving oral anticoagulation therapy such as Coumadin or Warfarin. The cartridge is to be used with the i-Stat 1 Analyzer…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0441-2014·2013-12-11
Boston Scientific Recalls Navigator HD Ureteral Access Sheath Sets
Boston Scientific is recalling Navigator HD Ureteral Access Sheath Sets because the dilator tip may separate from the body.
Product
Navigator HD l3F/15F x 36cm Ureteral Access Sheath Set Product No M0062502280, RDF Catalog No 250-228, Sterile. Indicated for use in endoscopic procedures to facilitate the passage of endoscopes, urological instruments and for the injection of fluids into the urinary tract.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0453-2014·2013-12-11
Sunrise Zippie Voyage Stroller Recalled for Potential Seat Dislodgement
Sunrise Medical is recalling Zippie Voyage strollers because a plastic latch may deform, allowing the seat to dislodge and causing the occupant to slide out.
Product
Sunrise Brand Zippie Voyage, Chair with Casters, Early Intervention Device (Stroller), Model: EIZ14; Product is manufactured and distributed by Sunrise Medical (US) LLC., Fresno, CA. Used by a person to move from one place to another while sitting.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0442-2014·2013-12-11
Boston Scientific Recalls Navigator HD Ureteral Access Sheath Sets
Boston Scientific is recalling 449 units of Navigator HD Ureteral Access Sheath Sets because the dilator tip may separate from the body.
Product
Navigator HD l3F/15F x 46cm Ureteral Access Sheath Set Product No M0062502280, RDF Catalog M0062502290, Sterile. Indicated for use in endoscopic procedures to facilitate the passage of endoscopes, urological instruments and for the injection of fluids into the urinary tract.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0455-2014·2013-12-11
Synthes Zero-P VA Implant Recalled for Potential Screw Back-Out Risk
Synthes USA is recalling specific Zero-P VA implants because a screw could back out if the blocking mechanism is not visually confirmed to cover the screw head.
Product
Synthes Zero-P VA Implant 7 MM Height Parallel Sterile The Synthes Zero-P VA Implant 7 MM Height Parallel Sterile is a stand alone anterior cervical interbody fusion device indicated for use in skeletally mature patients with degenerative disc disease (DDD) with accompanying…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0436-2014·2013-12-11
Intuitive Surgical Recalls da Vinci Patient Side Manipulator Assemblies
Intuitive Surgical is recalling 1,386 da Vinci Patient Side Manipulator assemblies due to friction that can cause instrument motion to stall and catch up.
Product
Assembly, Patient Side Manipulator on da Vinci Surgical Systems: da Vinci S Surgical System; da Vinci SI Surgical System da Vinci Si-e Surgical System; Manufactured by Intuitive Surgical Sunnyvale, CA 94086. The Intuitive Surgical Endoscopic Instrument Control System…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0454-2014·2013-12-11
GE Centricity Web Software Recalled for Patient Safety Concerns
GE Healthcare is recalling Centricity Web software due to an issue with rejected images that may impact patient safety.
Product
The GE Centricity Web; Software Version 3.0x, is intended for use under the direct supervision of a licensed healthcare practitioner. The Centricity Enterprise Web is an image and information distribution system for the clinical review of medical images and reports. The…
Category
Medical Device
Distribution
13 states
HighFDA (Devices)·Z-0440-2014·2013-12-11
Boston Scientific Recalls Navigator HD Ureteral Access Sheath Sets
Boston Scientific is recalling 274 units of Navigator HD Ureteral Access Sheath Sets because the dilator tip may separate from the body.
Product
Navigator HD l3F/15F x 28 cm Ureteral Access Sheath Set Product No M0062502270, RDF Catalog No 250-227, Sterile. Indicated for use in endoscopic procedures to facilitate the passage of endoscopes, urological instruments and for the injection of fluids into the urinary tract.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0433-2014·2013-12-11
Siemens syngo Lab Data Manager Software Recall for Auto-verification Failures
Siemens Healthcare Diagnostics is recalling syngo Lab Data Manager software versions VA11B and VA12A because the system may release results that require manual review or delay result transmission.
Product
syngo(R) Lab Data Manager - Version VA11B and VA12A Systems Securely consolidates data from multiple lab instruments, the LIS and Siemens StreamLAB(R) Automation Solutions. It provides autoverification, integrated QC capabilities, browser-based connectivity supporting up to…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0432-2014·2013-12-11
Olympus Recalls Thunderbeat Surgical Instruments Due to Component Damage
Olympus America Inc. is recalling Thunderbeat surgical instruments because they may crack, break, or deform during use.
Product
TB-0545PC: THUNDERBEAT 5 mm , 45 em, Pistol Grip TB-0535PC: THUNDERBEAT 5 mm, 35 em, Pi stol Grip TB-0545IC: THUNDERBEAT 5 mm, 45 em, In line Grip TB-0535IC: THUNDERBEAT 5 mm, 35 em, Inline Grip TB-0520IC: THUNDERBEAT 5 mm, 20 em, In line Grip TB-051 OIC: THUNDERBEAT 5 mm, I 0…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0421-2014·2013-12-04
DePuy Orthopaedics Recalls HP M.B.T. Keel Punch Knee Instruments
DePuy Orthopaedics is voluntarily recalling HP M.B.T. Keel Punch Knee Instruments because tabs on the connection end may fracture and remain in the patient.
Product
SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT PUNCH NONCEMENTED Size 1-1.5 HP M.B.T. Keel Punch Knee Instrument is used to prepare the proximal tibial canal geometry to accept the final or definitive tibial tray used during total knee arthroplasty.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0415-2014·2013-12-04
DePuy Recalls HP M.B.T. Keel Punch Knee Instruments Due to Fracture Risk
DePuy Orthopaedics is voluntarily recalling HP M.B.T. Keel Punch Knee Instruments because tabs on the connection end may fracture and be left in the patient.
Product
SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT KEEL PUNCH NONCEMENTED Size 1-1.5 HP M.B.T. Keel Punch Knee Instrument is used to prepare the proximal tibial canal geometry to accept the final or definitive tibial tray used during total knee arthroplasty.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0423-2014·2013-12-04
DePuy Orthopaedics Recalls HP M.B.T. Keel Punch Knee Instruments
DePuy Orthopaedics is voluntarily recalling HP M.B.T. Keel Punch Knee Instruments because tabs on the connection end may fracture and remain in the patient.
Product
SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT PUNCH NONCEMENTED Size 4-7 HP M.B.T. Keel Punch Knee Instrument is used to prepare the proximal tibial canal geometry to accept the final or definitive tibial tray used during total knee arthroplasty.
Category
Medical Device
Distribution
Distributed nationwide

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25751–25775 of 27722