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The James Skinner Co.

The James Skinner Co. Recalls

All product recalls associated with The James Skinner Co..

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Recall Summary

Total Recalls

1000

Past Year

731

Class I (Serious)

175

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 1201–1220 of 11123 recalls

Cinnamon Pecan Braid (Marketside) – Unlabeled Pecans (2024)

Product has incorrect back label that does not declare pecans are present in the product.

Class IIModerate

FDAApr 11, 2024Nationwide• The James Skinner Co.

King Kullen Broccoli Cutlets (Gracie's Kitchens) – Undeclared Wheat (2024)

Undeclared Gluten

Product contains undeclared wheat and sesame.

Class IHigh

FDAApr 9, 2024NY• Gracie's Kitchens Inc.

Samaritan PAD Defibrillator (HeartSine) – Voice Prompt Malfunction (2024)

Automated external defibrillators have a manufacturing issue that could prevent the device from delivering instructional voice prompts to the user during use of the device. Visual instructional icons will still be present, but this issue could potentially lead to no therapy or a delay in therapy.

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Moderate

FDAApr 8, 2024Nationwide• HeartSine Technologies Ltd 207 Airport Road West Belfast United Kingdom

CARESCAPE Canvas 1000 (GE Healthcare) – Monitoring Loss Risk (2024)

GE HealthCare has become aware of the potential for loss of monitoring on CARESCAPE Canvas 1000, CARESCAPE Canvas Smart Display, and certain versions of CARESCAPE B850 and CARESCAPE B650 monitors if, following the replacement of the CPU timekeeper battery, a mains power loss occurs during active monitoring. In the unlikely event that this occurs, it can result in the displays or monitors not turning on, after the mains power is restored. This can result in a delay in recognizing changes in patient condition until a replacement monitor is connected.

Moderate

FDAApr 5, 2024Nationwide• GE Healthcare Finland Oy Kuortaneenkatu 2 Helsinki Finland

Urinalysis Test Strips (Macherey Nagel) – Missing Test Pad (2024)

The reason for the recall is one of the test pads, for the parameter leukocytes, was missing on some of the test strips. The issue was identified by a consumer by way of a Henry Schein Inc. (HSI) customer complaint. This problem can potentially result in the possibility that the parameter leucocytes (a non-specific marker for urinary track infections and an indicator for inflammatory renal processes) is interpreted instrumentally as a false negative. The following HSI item number and lot number were affected: Urispec 11-Way, #102-2285, LOT 65402.

Low

FDAApr 4, 2024Nationwide• Macherey Nagel Gmbh & Co. Kg Valencienner Str. 11 Duren Germany

Scopis ENT Software (Stryker) – Visual Feedback Misalignment (2024)

Unreleased software was installed on customer systems resulting in the visual feedback on the screen to show the points to be off from the physical reference point of the pointer or suction.

Low

FDAApr 4, 2024Nationwide• Stryker Leibinger GmbH & Co. KG Botzinger Str. 41 Freiburg Im Breisgau Germany

Distal Access Catheter (Stryker) – Unspecified Recall Reason (2024)

Stryker Neurovascular is recalling their DAC- Distal Access Catheter -038 136cm, a Distal Access Catheter by removal. The reason for the recall is: the DAC Lot #0000486382 was released with out-of-specification endotoxin results.

Low

FDAApr 3, 2024Nationwide• Stryker Neurovascular

Airvo 2 Humidifier (Fisher & Paykel) – Speaker Configuration (2024)

Humidifier devices, used to deliver high flow respiratory therapy to patients, manufactured before 14 August 2017, have a speaker configuration that may result in distorted, intermittent or inaudible alarm sound levels. In the absence of an audible alarm, if there is an interruption to therapy, a patient may experience oxygen desaturation.

Moderate

FDAApr 2, 2024Nationwide• Fisher & Paykel Healthcare, Ltd. 15 Maurice Paykel Place East Tamaki Auckland New Zealand

EchoTip Ultrasound Needle (Cook) – Bacterial Endotoxin Levels (2024)

Devices may contain elevated levels of bacterial endotoxin.

Low

FDAApr 1, 2024IN• Cook Medical Incorporated

EchoTip Ultrasound Needle (Cook) – Bacterial Endotoxin Levels (2024)

Devices may contain elevated levels of bacterial endotoxin.

Low

FDAApr 1, 2024IN• Cook Medical Incorporated

LASER Application Instrument (Karl Storz) – Sterilization Concern (2024)

Laser surgical instruments have no specific evidence of a validated reprocessing method, therefore these instruments lack sterility assurance, so once the instruments have gone through reprocessing after use and then are used again, there is an increased risk of the patient being exposed to infection.

Moderate

FDAApr 1, 2024Nationwide• Karl Storz Endoscopy