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Medimaps Group Fongit Chemin des Aulx 18 Plan-les-Ouates Switzerland

Medimaps Group Fongit Chemin des Aulx 18 Plan-les-Ouates Switzerland Recalls

All product recalls associated with Medimaps Group Fongit Chemin des Aulx 18 Plan-les-Ouates Switzerland.

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Recall Summary

Total Recalls

1000

Past Year

123

Class I (Serious)

Most Recent

Nov 2025

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 121–140 of 2383 recalls

TBS iNsight (Medimaps) – calculation variability (2025)

Potential variability in calculations from fast array scans compared to array scans when operating on Hologic Horizon machines.

Low

FDAFeb 3, 2025AL, AZ, CA +21 more• Medimaps Group Fongit Chemin des Aulx 18 Plan-les-Ouates Switzerland

Gerber Soothe 'n' Chew Teething Sticks Strawberry Apple (Nestle) – Choking Risk (2025)

Choking Hazard

Firm received complaints of infant choking.

Class IHigh

FDAJan 31, 2025AL, AZ, AR +43 more• Nestle-USA, Inc. (Corporate Office)

Gerber Soothe 'n' Chew Teething Sticks Banana (Nestle) – Choking Risk (2025)

Choking Hazard

Firm received complaints of infant choking.

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Class I

High

FDAJan 31, 2025AL, AZ, AR +43 more• Nestle-USA, Inc. (Corporate Office)

Guaifenesin Codeine Solution (PAI Holdings) – Superpotent Preservative (2025)

Superpotent; sodium benzoate preservative

Class IIILow

FDAJan 7, 2025OH• PAI Holdings, LLC. dba Pharmaceutical Associates Inc

Chocolate Caramels (V Chocolates) – Plastic Fragments (2024)

Small pieces of plastic broken tray in the product.

Class IIModerate

FDADec 30, 2024Nationwide• V Chocolates, Inc

Green Chile Bean Burrito (Mi Ranchito) – Undeclared Milk (2024)

Milk not listed in the ingredients or included in parentheses after American Cheese.

Class IIModerate

FDADec 27, 2024IN, NM• Mi Ranchito Foods, Incorporated

AnchorFast Guard Select Tube Fastener (Hollister) – Skin Barrier Wear Time (2024)

Hollister received reports of decreased skin barrier wear time which could can lead to tube migration

Moderate

FDADec 23, 2024Nationwide• Hollister Incorporated

AnchorFast SlimFit Tube Fastener (Hollister) – Skin Barrier Wear Time (2024)

Hollister received reports of decreased skin barrier wear time which could can lead to tube migration

Moderate

FDADec 23, 2024Nationwide• Hollister Incorporated

CyberKnife Treatment System (Accuray) – Snap Ring Detachment (2024)

Snap rings may become partially or completed detached from the shafts within the internal mechanism. Uncontrolled rotation may occur on the left and right roll axes when the rings are removed or damaged.

Moderate

FDADec 23, 2024Nationwide• Accuray Incorporated

AnchorFast Oral Endotracheal Tube Fastener (Hollister) – Skin Barrier Wear Time (2024)

Hollister received reports of decreased skin barrier wear time which could can lead to tube migration

Moderate

FDADec 23, 2024Nationwide• Hollister Incorporated

AnchorFast Guard Tube Fastener (Hollister) – Skin Barrier Wear Time (2024)

Hollister received reports of decreased skin barrier wear time which could can lead to tube migration

Moderate

FDADec 23, 2024Nationwide• Hollister Incorporated

Alpha Test (Iovate) - Cathine Presence (2024)

Presence of cathine in product

Class IIModerate

FDADec 18, 2024AZ, CA, CO +27 more• Iovate Health Sciences USA Inc.

Calibrate CCX Interbody System (Alphatec) – Implant Collapse Risk (2024)

Complaints have been received regarding post-operative implant collapse.

Moderate

FDADec 15, 2024Nationwide• Alphatec Spine, Inc. 1950 Camino Vida Roble

Esteem Synergy Skin Barrier (ConvaTec) – Incorrect Wafer Size (2024)

Laceration Risk

Ostomy skin barrier package contains a pre-cut wafer of 28mm instead of 16mm and/or 35mm pre-cut wafers, as stated package labeling. If pre-cut wafers are too big the device cannot be used and if the pre-cut wafer is too small and the device user tries to apply, this could cause abrasion, stomal cut, and bleeding

High

FDANov 29, 2024IL, NY, OH• ConvaTec, Inc

Eclipse PRO Holter Recorder (Spacelabs) – Serial Number Error (2024)

Due to a manufacturing error the incorrect device serial number was potentially programmed into the holter recorder. The physical serial number label on the device might not match the serial number programmed into the device.

Low

FDANov 25, 2024AR, CA, CO +19 more• Spacelabs Healthcare, Ltd. Unit B Foxholes Centre; John Tate Road Hertford United Kingdom