Browse the most recent U.S. safety recalls in our connected official government data.
3,525 recalls in our current data. Showing 1,201–1,300, newest first.
Incorrect labeling- The labeled box for the Large Esophageal Flange contains a Large Esophageal and Tracheal Flange, and the labeled box for the Large Esophageal and Tracheal Flang…
Company / brand: Freudenberg Medical recalls
Official ID Z-2910-2026 · Official record ↗
Incorrect labeling- The labeled box for the Large Esophageal Flange contains a Large Esophageal and Tracheal Flange, and the labeled box for the Large Esophageal and Tracheal Flang…
Company / brand: Freudenberg Medical recalls
Official ID Z-2909-2026 · Official record ↗
Currently labeled shelf life of 36 months is not substantiated by real-time data. Devices will be relabeled to reflect revised shelf life of 26 months. The use of a medical device …
Company / brand: TISSIUM SA recalls
Official ID Z-2908-2026 · Official record ↗
Currently labeled shelf life of 36 months is not substantiated by real-time data. Devices will be relabeled to reflect revised shelf life of 26 months. The use of a medical device …
Company / brand: TISSIUM SA recalls
Official ID Z-2907-2026 · Official record ↗
Currently labeled shelf life of 36 months is not substantiated by real-time data. Devices will be relabeled to reflect revised shelf life of 26 months. The use of a medical device …
Company / brand: TISSIUM SA recalls
Official ID Z-2906-2026 · Official record ↗
Currently labeled shelf life of 36 months is not substantiated by real-time data. Devices will be relabeled to reflect revised shelf life of 26 months. The use of a medical device …
Company / brand: TISSIUM SA recalls
Official ID Z-2905-2026 · Official record ↗
Currently labeled shelf life of 36 months is not substantiated by real-time data. Devices will be relabeled to reflect revised shelf life of 26 months. The use of a medical device …
Company / brand: TISSIUM SA recalls
Official ID Z-2904-2026 · Official record ↗
Currently labeled shelf life of 36 months is not substantiated by real-time data. Devices will be relabeled to reflect revised shelf life of 26 months. The use of a medical device …
Company / brand: TISSIUM SA recalls
Official ID Z-2903-2026 · Official record ↗
Currently labeled shelf life of 36 months is not substantiated by real-time data. Devices will be relabeled to reflect revised shelf life of 26 months. The use of a medical device …
Company / brand: TISSIUM SA recalls
Official ID Z-2902-2026 · Official record ↗
Currently labeled shelf life of 36 months is not substantiated by real-time data. Devices will be relabeled to reflect revised shelf life of 26 months. The use of a medical device …
Company / brand: TISSIUM SA recalls
Official ID Z-2901-2026 · Official record ↗
The active ingredient concentration in the lysing bag solution of specific GEM Premier 5000 lots did not meet established manufacturing specifications. The malfunction could result…
Company / brand: Instrumentation Laboratory recalls
Official ID Z-2900-2026 · Official record ↗
The active ingredient concentration in the lysing bag solution of specific GEM Premier 7000 with iQM3 PAK lots did not meet established manufacturing specifications. The malfunctio…
Company / brand: Instrumentation Laboratory recalls
Official ID Z-2899-2026 · Official record ↗
Due to a design issue causing the incorrect engraved numbering on implant that could result in the incorrect orientation of the implant.
Company / brand: United Orthopedic recalls
Official ID Z-2898-2026 · Official record ↗
Due to a design issue causing the incorrect engraved numbering on implant that could result in the incorrect orientation of the implant.
Company / brand: United Orthopedic recalls
Official ID Z-2897-2026 · Official record ↗
Stability issues with the reconstituted lyophilized human plasma and bivalirudin matrix have been identified. These stability issues lead to a degradation of measurable bivalirudin…
Company / brand: Aniara Diagnostica recalls
Official ID Z-2896-2026 · Official record ↗
Stability issues with the reconstituted lyophilized human plasma and bivalirudin matrix have been identified. These stability issues lead to a degradation of measurable bivalirudin…
Company / brand: Aniara Diagnostica recalls
Official ID Z-2895-2026 · Official record ↗
Stability issues with the reconstituted lyophilized human plasma and bivalirudin matrix have been identified. These stability issues lead to a degradation of measurable bivalirudin…
Company / brand: Aniara Diagnostica recalls
Official ID Z-2894-2026 · Official record ↗
Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Official ID Z-2893-2026 · Official record ↗
Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Official ID Z-2892-2026 · Official record ↗
Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Official ID Z-2891-2026 · Official record ↗
Processing of urine albumin assay on the CI analyzers may lead to the following issues: Falsely depressed Atellica CH Urea Nitrogen (UN_c) results; Falsely depressed Atellica CH En…
Company / brand: Siemens Healthcare Diagnostics recalls
Official ID Z-2890-2026 · Official record ↗
Analyzers contain incorrect algorithms which may affect antimicrobial susceptibility test results, leading to false susceptibility classifications."
Company / brand: Beckman Coulter recalls
Official ID Z-2889-2026 · Official record ↗
Analyzers contain incorrect algorithms which may affect antimicrobial susceptibility test results, leading to false susceptibility classifications."
Company / brand: Beckman Coulter recalls
Official ID Z-2888-2026 · Official record ↗
Due to incorrect cartridges include in affected products that there is the potential for false-susceptible or false-resistant susceptibility results and may lead to selection of an…
Company / brand: Hardy Diagnostics recalls
Official ID Z-2887-2026 · Official record ↗
Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail.
Company / brand: United Orthopedic recalls
Official ID Z-2886-2026 · Official record ↗
Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail.
Company / brand: United Orthopedic recalls
Official ID Z-2885-2026 · Official record ↗
Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail.
Company / brand: United Orthopedic recalls
Official ID Z-2884-2026 · Official record ↗
Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail.
Company / brand: United Orthopedic recalls
Official ID Z-2883-2026 · Official record ↗
This recall is retroactively being reported. Refurbished bassinets failed to meet quality standards prior to distribution.
Company / brand: Happiest Baby recalls
Official ID Z-2882-2026 · Official record ↗
out-of-specification sodium azide concentration in Syva Emit Tox Serum Tricyclic Antidepressant Calibrator/Controls Lot U2. While the assay results were not impacted, the overall h…
Company / brand: Siemens Healthcare Diagnostics recalls
Official ID Z-2881-2026 · Official record ↗
Out-of-specification sodium azide concentration in Syva Emit Disopyramide Enzyme Immunoassay Calibrator Lot U1. While the assay results were not impacted, the overall health risk t…
Company / brand: Siemens Healthcare Diagnostics recalls
Official ID Z-2880-2026 · Official record ↗
Spinal cord stimulation system lead body may be exposed to stress at the anchor site. This may result in high impedance measurements or lead fractures, which may lead to inadequate…
Company / brand: Boston Scientific Neuromodulation recalls
Official ID Z-2879-2026 · Official record ↗
A software vulnerability may allow unauthorized persons to gain privileged access to the device, which could result in loss of patient monitoring, missed patient alarms, and/or acc…
Company / brand: GE Medical Systems Information Technologies recalls
Official ID Z-2878-2026 · Official record ↗
Firm has identified mismatches between the outbreak strain and the reference strain used in the development of its qualitative, multiplexed, nucleic acid-based in vitro diagnostic …
Company / brand: Biofire Defense recalls
Official ID Z-2877-2026 · Official record ↗
Software issue issue with the MAC VU360 v3.0 system. After selecting the order refresh icon, an open preview or review screen might fail to close automatically after 2 minutes of i…
Company / brand: GE Medical Systems Information Technologies recalls
Official ID Z-2876-2026 · Official record ↗
Thumbnails from a previously opened patient study may be displayed in the Thumbnail Bar while a different patient study is currently open.
Company / brand: Merge Healthcare recalls
Official ID Z-2875-2026 · Official record ↗
Thumbnails from a previously opened patient study may be displayed in the Thumbnail Bar while a different patient study is currently open.
Company / brand: Merge Healthcare recalls
Official ID Z-2874-2026 · Official record ↗
Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier packaging damage caused…
Company / brand: Biomet recalls
Official ID Z-2871-2026 · Official record ↗
Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier packaging damage caused…
Company / brand: Biomet recalls
Official ID Z-2870-2026 · Official record ↗
Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier packaging damage caused…
Company / brand: Biomet recalls
Official ID Z-2869-2026 · Official record ↗
Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier packaging damage caused…
Company / brand: Biomet recalls
Official ID Z-2868-2026 · Official record ↗
Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier packaging damage caused…
Company / brand: Biomet recalls
Official ID Z-2867-2026 · Official record ↗
There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
Company / brand: Stryker recalls
Official ID Z-2866-2026 · Official record ↗
There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
Company / brand: Stryker recalls
Official ID Z-2865-2026 · Official record ↗
There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
Company / brand: Stryker recalls
Official ID Z-2864-2026 · Official record ↗
There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
Company / brand: Stryker recalls
Official ID Z-2863-2026 · Official record ↗
There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
Company / brand: Stryker recalls
Official ID Z-2862-2026 · Official record ↗
Due to a software issue which may result in false co-infection (e.g., Positive for Flu A, when SARS-CoV-2 is present).
Company / brand: Nuclein recalls
Official ID Z-2861-2026 · Official record ↗
Events observed where anesthetic agent was not delivered when the vaporizer was activated. Failure to deliver the anesthetic agent may result in the patient receiving insufficient …
Company / brand: Maquet Critical Care AB recalls
Official ID Z-2860-2026 · Official record ↗
Pedicle screw system intended to provide immobilization/stabilization of spinal segments as adjunct to thoracic/lumbar/sacral spine fusion may have anti-torque instrument with unde…
Company / brand: Innovasis recalls
Official ID Z-2859-2026 · Official record ↗
Convenience kits contain needle free access device that has an improper seal which may result in doming or tearing of the silicone seal.
Company / brand: Medical Action Industries recalls
Official ID Z-2858-2026 · Official record ↗
Due to a defective circuit board that overheats
Company / brand: Oxos Medical recalls
Official ID Z-2857-2026 · Official record ↗
A software issue may cause the wheelchair's driving mechanism to fall out of calibration. When this occurs, the device may experience unexpected steering drift or imprecise control…
Company / brand: MUNEVO recalls
Official ID Z-2856-2026 · Official record ↗
Potential for the batter to have a thermal-runway event during charging, resulting in smoke and odor.
Company / brand: THERANICA BIOELECTRONICS recalls
Official ID Z-2855-2026 · Official record ↗
Due to a software issue within the WebApp that potentially prevents the user to overwrite the results.
Company / brand: Copan WASP recalls
Official ID Z-2854-2026 · Official record ↗
If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the…
Company / brand: Pride Mobility Products recalls
Official ID Z-2853-2026 · Official record ↗
If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the…
Company / brand: Pride Mobility Products recalls
Official ID Z-2852-2026 · Official record ↗
If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the…
Company / brand: Pride Mobility Products recalls
Official ID Z-2851-2026 · Official record ↗
If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the…
Company / brand: Pride Mobility Products recalls
Official ID Z-2850-2026 · Official record ↗
If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the…
Company / brand: Pride Mobility Products recalls
Official ID Z-2849-2026 · Official record ↗
If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the…
Company / brand: Pride Mobility Products recalls
Official ID Z-2848-2026 · Official record ↗
If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the…
Company / brand: Pride Mobility Products recalls
Official ID Z-2847-2026 · Official record ↗
If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the…
Company / brand: Pride Mobility Products recalls
Official ID Z-2846-2026 · Official record ↗
If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the…
Company / brand: Pride Mobility Products recalls
Official ID Z-2845-2026 · Official record ↗
If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the…
Company / brand: Pride Mobility Products recalls
Official ID Z-2844-2026 · Official record ↗
If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the…
Company / brand: Pride Mobility Products recalls
Official ID Z-2843-2026 · Official record ↗
If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the…
Company / brand: Pride Mobility Products recalls
Official ID Z-2842-2026 · Official record ↗
If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the…
Company / brand: Pride Mobility Products recalls
Official ID Z-2841-2026 · Official record ↗
Potential for breach in sterile barrier of device packaging.
Company / brand: Boston Scientific recalls
Official ID Z-2840-2026 · Official record ↗
Potential for breach in sterile barrier of device packaging.
Company / brand: Boston Scientific recalls
Official ID Z-2839-2026 · Official record ↗
Potential for breach in sterile barrier of device packaging.
Company / brand: Boston Scientific recalls
Official ID Z-2838-2026 · Official record ↗
Devices could potentially contain an occluded or partially occluded Guedel Airway tip.
Company / brand: INTEGRATED MEDCRAFT recalls
Official ID Z-2837-2026 · Official record ↗
Devices could potentially contain an occluded or partially occluded Guedel Airway tip.
Company / brand: INTEGRATED MEDCRAFT recalls
Official ID Z-2836-2026 · Official record ↗
Charging cradle for the device may overheat while charging the device's removable battery pack, presenting risk of thermal event (fire). Firm has received reports alleging the prod…
Company / brand: Therabody recalls
Official ID Z-2835-2026 · Official record ↗
Due to software issues where does not handle combo assay results. The software may replace the final combo test result with one of the sub-results resulting in incorrect reporting …
Company / brand: Beckman Coulter Biomedical recalls
Official ID Z-2834-2026 · Official record ↗
Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates within fluid path of the Manifol…
Company / brand: AVID Medical recalls
Official ID Z-2798-2026 · Official record ↗
Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates within fluid path of the Manifol…
Company / brand: AVID Medical recalls
Official ID Z-2797-2026 · Official record ↗
Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates within fluid path of the Manifol…
Company / brand: AVID Medical recalls
Official ID Z-2796-2026 · Official record ↗
undeclared egg
Company / brand: Blank Slate Creamery Production recalls
Official ID H-1272-2026 · Official record ↗
Undeclared allergen (egg)
Company / brand: Kerry recalls
Official ID H-1237-2026 · Official record ↗
Nitrofurans detected in product
Company / brand: CAMPO RICO FOODS recalls
Official ID H-1236-2026 · Official record ↗
Possible foreign object (thin, soft plastic strands).
Company / brand: PT Organics recalls
Official ID H-1223-2026 · Official record ↗
Possible Salmonella in Moringa Leaf Powder product.
Company / brand: FACTORY6 recalls
Official ID H-1222-2026 · Official record ↗
Product label allergen "contains" statement does not include anchovy(fish)
Company / brand: JINA F&C recalls
Official ID H-1221-2026 · Official record ↗
Products may be contaminated with Listeria monocytogenes.
Company / brand: La Colonia Foods recalls
Official ID H-1220-2026 · Official record ↗
Products may be contaminated with Listeria monocytogenes.
Company / brand: La Colonia Foods recalls
Official ID H-1219-2026 · Official record ↗
Products may be contaminated with Listeria monocytogenes.
Company / brand: La Colonia Foods recalls
Official ID H-1218-2026 · Official record ↗
Products may be contaminated with Listeria monocytogenes.
Company / brand: La Colonia Foods recalls
Official ID H-1217-2026 · Official record ↗
Product contaminated with Listeria monocytogenes.
Company / brand: Clover Hill Dairy recalls
Official ID H-1216-2026 · Official record ↗
Product contaminated with Listeria monocytogenes.
Company / brand: Clover Hill Dairy recalls
Official ID H-1215-2026 · Official record ↗
Product contaminated with Listeria monocytogenes.
Company / brand: Clover Hill Dairy recalls
Official ID H-1214-2026 · Official record ↗
Product contaminated with Listeria monocytogenes.
Company / brand: Clover Hill Dairy recalls
Official ID H-1213-2026 · Official record ↗
Product contaminated with Listeria monocytogenes.
Company / brand: Clover Hill Dairy recalls
Official ID H-1212-2026 · Official record ↗
Product contaminated with Listeria monocytogenes.
Company / brand: Clover Hill Dairy recalls
Official ID H-1211-2026 · Official record ↗
Product contaminated with Listeria monocytogenes.
Company / brand: Clover Hill Dairy recalls
Official ID H-1210-2026 · Official record ↗
Product contaminated with Listeria monocytogenes.
Company / brand: Clover Hill Dairy recalls
Official ID H-1209-2026 · Official record ↗
Product contaminated with Listeria monocytogenes.
Company / brand: Clover Hill Dairy recalls
Official ID H-1208-2026 · Official record ↗
Product contaminated with Listeria monocytogenes.
Company / brand: Clover Hill Dairy recalls
Official ID H-1207-2026 · Official record ↗
Product contaminated with Listeria monocytogenes.
Company / brand: Clover Hill Dairy recalls
Official ID H-1206-2026 · Official record ↗
Product contaminated with Listeria monocytogenes.
Company / brand: Clover Hill Dairy recalls
Official ID H-1205-2026 · Official record ↗
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Government sources last checked October 22, 2026 at 12:00 PM UTC.