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In2Bones, SAS 28 Chemin du petit Bois Ecully France

In2Bones, SAS 28 Chemin du petit Bois Ecully France Recalls

All product recalls associated with In2Bones, SAS 28 Chemin du petit Bois Ecully France.

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Recall Summary

Total Recalls

1000

Past Year

295

Class I (Serious)

116

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 581–600 of 4465 recalls

I.B.S Compression Screw (In2Bones) – Batch Mix-up (2024)

This Field Action is being conducted following the identification of a batch mix-up between I.B.S Compression screws diameter 6.5mm length 75mm and I.B.S Compression screws diameter 6.5mm length 80mm. The screws of the batches concerned by the recall may have different lengths from those issued on their labels.

FDAJan 26, 2024Nationwide• In2Bones, SAS 28 Chemin du petit Bois Ecully France

Epidural Tray (B. Braun) – Connector Compatibility Issue (2024)

Kits should contain Filter Straws with Standard Luer Connections however the kits contain Filter Straws with Neuraxial connectors preventing interface with the other components of the kit.

FDAJan 22, 2024Nationwide• B. Braun Medical, Inc.

W&H Surgical Handpiece (W&H) – Laser Marking Error (2024)

1:2 speed increasing surgical handpieces have been incorrectly laser marked during production. The specific laser marking should read 1:2, but instead it reads 1:1 on the body of the handpiece

1...28 293031 32...224

Page 30 of 224Next

FDAJan 16, 2024Nationwide• W & H DENTALWERK BUERMOOS GMBH Ignaz Glaser Strase 53 53 IGNAZ-GLASER-STRASSE BUERMOOS Austria

Methylfolate Chewables (Bluebonnet) – Label Error (2024)

Label error during reprint. Says 1000 mg instead of 1000 mcg on the center front panel of the label.

Class IIILow

FDAJan 12, 2024Nationwide• Bluebonnet Nutrition Corporation (Dairy Ashford)

Custodiol HTK Solution (Dr. Franz Koehler) – Particle Presence (2024)

Potential for particles to be present in solution.

FDAJan 9, 2024Nationwide• Dr Franz Koehler Chemie Gmbh Werner-Von-Siemens-Str. 14-28 Bensheim Germany

Benny T's Dry Hot Sauce (Vesta) – Unlisted Ingredients (2024)

The firm was notified by the North Carolina Dept of Agriculture and Consumer Services that the product labeling does not include wheat and other ingredient common names in the ingredient statement.

Class IIModerate

FDAJan 8, 2024AL, AZ, CA +21 more• Benny Ts Vesta Inc dba Vesta Firey Gourmet Toppings

Benny T's Dry Hot Sauce Scorpion (Vesta) – Unlisted Ingredients (2024)

The firm was notified by the North Carolina Dept of Agriculture and Consumer Services that the product labeling does not include wheat and other ingredient common names in the ingredient statement.

Class IIModerate

FDAJan 8, 2024AL, AZ, CA +21 more• Benny Ts Vesta Inc dba Vesta Firey Gourmet Toppings

Benny T's Dry Hot Sauce Very Hot (Vesta) – Unlisted Ingredients (2024)

The firm was notified by the North Carolina Dept of Agriculture and Consumer Services that the product labeling does not include wheat and other ingredient common names in the ingredient statement.

Class IIModerate

FDAJan 8, 2024AL, AZ, CA +21 more• Benny Ts Vesta Inc dba Vesta Firey Gourmet Toppings

Allura Xper X-ray Systems (Philips) – Framegrabber Performance Issue (2024)

Framegrabber card may not perform as intended. Monitor may show no viewports, or show one or more viewports may show no image, a distorted image, or a frozen image. Switching between viewports on the monitor may not be possible. Issue may result in delay of procedure.

FDAJan 2, 2024Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

AQUABILITI AQUASTAT (MRP) – sodium chloride issues (2023)

The saline flush syringes may fail to meet USP criteria for stated sodium chloride content after 12 months.

FDADec 28, 2023Nationwide• MRP, LLC dba Aquabiliti

BlendJet 2 Portable Blenders – fire risk (2023)

Fire/Burn Risk

This recall involves BlendJet 2 Portable Blenders sold in a variety of colors and designs. Serial numbers are printed on the bottom of the base along with "blendjet2" and "The Original Portable Blender." The blenders measure approximately 9.5 inches in height and 3 inches in width and weigh approximately 1.5 pounds. Units where the first 4 digits of the serial number are between 5201-5542 and are subject to the recall must be identified through the use of the "Is my BlendJet 2 Recalled?" tool located at www.blendjet.com/safetyandrecall.

CPSCDec 28, 2023Nationwide• BlendJet Inc., of Benicia, California

GE Voluson Probe (GE Healthcare) – image artifact risk (2023)

GE HealthCare has become aware of an issue with certain IC9-RS ultrasound probes (see Affected Products List) that can result in a double image artifact creating a ghost image with realistic features. An unrecognized artifact may lead to misdiagnosis.

Undeclared Allergen

Undeclared Allergens - Milk and Soy

Class IHigh

FDADec 15, 2023AZ, AR, CA +30 more• Eban's Bakehouse LLC