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Stryker Instruments Div. of Stryker Corporation

Stryker Instruments Div. of Stryker Corporation Recalls

All product recalls associated with Stryker Instruments Div. of Stryker Corporation.

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Recall Summary

Total Recalls

1000

Past Year

726

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 7621–7640 of 11124 recalls

Flyte Togas (Stryker Instruments) – incorrect expiration date (2014)

A single lot (11121171) of Flyte Toga Peel-away X-Large (catalog number 0408-830-100) was labeled with an incorrect expiration date of 2412-12-01. The correct expiration date should have read 2014-12-01.

Class IIILow

FDADec 22, 2014Nationwide• Stryker Instruments Div. of Stryker Corporation

Focal Sim Treatment Planning System (Elekta) – CT measurement error (2014)

Incorrect CT to ED when using the Monaco Image Statistics Tool.

Class IIModerate

FDADec 19, 2014Nationwide• Elekta, Inc.

McKesson Cardiology ECG Management (McKesson Israel) – timestamp error (2014)

An ECG procedure time stamp is incorrect, due to a software error in the McKesson Cardiology ECG Management with software versions 13.1 and 13.1.1.

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Class IIModerate

FDADec 19, 2014MA, MS, NH +3 more• McKesson Israel Ltd.

Monaco Treatment Planning System (Elekta) – CT measurement error (2014)

Incorrect CT to ED when using the Monaco Image Statistics Tool.

Class IIModerate

FDADec 19, 2014Nationwide• Elekta, Inc.

BD 10 mL Syringe (Becton Dickinson) – stopper misalignment (2014)

The stopper of the 10mL BD Luer-Lok syringe is not properly seated in the syringe.

Class IIModerate

FDADec 19, 2014Nationwide• Becton Dickinson & Company

Mungbean Sprouts (Kkot Saem) - Listeria contamination (2014)

Listeria

Mungbean Sprouts are recalled because finished product was tested positive for Listeria monocytogenes.

Class IHigh

FDADec 19, 2014IN, OR, WA• Kkot Saem Bean Sprouts

Soybean Sprouts (Kkot Saem) - Listeria risk (2014)

Listeria

Soybean Sprouts are recalled because it has the potential to be contaminated with Listeria monocytogenes.

Class IHigh

FDADec 19, 2014IN, OR, WA• Kkot Saem Bean Sprouts

Animated Monkey Toy (Giggles International) – burn hazard (2014)

Fire/Burn Risk

This recall involves Giggles International Animated Sing-Along Monkey toys. The monkey is made of brown and beige plush material and is about 9 inches tall. The toy is designed to hold a song book titled "5 Little Monkeys" and to sing the song when activated. A red music note is on the bottom of the monkey's right foot and the face of a child with its hands covering its eyes are on the bottom of the monkey's left foot. Recalled sing-along monkeys were manufactured between 6/7/2014 and 7/5/2014 and have batch code GP1410028. The manufacture date in the M/D/YYYY format and batch code are printed on the bottom of a white fabric label attached near the base of the monkey's tail. The monkey toys came in a tan colored box with words "Animated Sing-Along Monkey," "Sing along with me!" and "I play peek-a-boo with you!" on the front. The age advisory "For ages 3+" and the warning that batteries are included are also on the front of the box.

CPSCDec 18, 2014Nationwide• Giggles International Ltd., of Hong Kong

Guava Filled Pastry (Vitony Bakery) – undeclared soy (2014)

Ingredients in label for "Pastelillos de Guayaba" (Guava Pastries) do not include soy lecithin.

Class IIModerate

FDADec 18, 2014PR• Vitony Bakery, Inc.

MEDPOR BARRIER Sheets (Stryker) – implant deformation risk (2014)

Potential for implant deformation, implant mechanical stability too low, loss of barrier adhesion intra-operatively, implant damage, implant cracking off/breaking intra-operatively.

Class IIModerate

FDADec 17, 2014Nationwide• Stryker Craniomaxillofacial Division

MEDPOR BARRIER Sheets (Stryker) – implant deformation risk (2014)

Potential for implant deformation, implant mechanical stability too low, loss of barrier adhesion intra-operatively, implant damage, implant cracking off/breaking intra-operatively.

Class IIModerate

FDADec 17, 2014Nationwide• Stryker Craniomaxillofacial Division

MEDPOR TITAN MAX Implant (Stryker) – incorrect article packaging (2014)

Article #81036 (MEDPOR Titan Max OFW - MTB - Right) reportedly contained article #81035 MEDPOR Titan Max OFW - MTB - Left. The appropriate articles were actually included in the shipment. However, the products had an incorrect barrier location.

Class IIModerate

FDADec 17, 2014Nationwide• Stryker Craniomaxillofacial Division

MEDPOR Surgical Chin Implant (Stryker) – potential damage risk (2014)

Potential for implant damage, implant cracking off/breaking intra-operatively.

Class IIModerate

FDADec 17, 2014Nationwide• Stryker Craniomaxillofacial Division

Roller Window Shades (WindowTex) – Injury Risk (2014)

This recall involves WindowTex custom-made fabric roller window shades that are raised and lowered by a side-mounted chain. The recalled shades have an idler with steel pin inserted into one end of the roller tube. The steel pin is used to connect the window shade to the metal mounting bracket. Roller shades included in this recall have idlers with model number D15T, used with a 1½-inch roller tube, and model number D20T, used with a 2-inch roller tube.

CPSCDec 16, 2014Nationwide• Windowcraft Inc. dba. WindowTex, of Garden City Park, NY

Veggie Sticks (Weis) – Incorrect Sodium Claims (2014)

Firm's sodium claims of 55 g/serving is incorrect. Product analyzed and found to contain shows 260 - 290 mg/serving size

Class IIILow

FDADec 16, 2014CT, ME, MA +5 more• Keystone Food Products Inc

Veggie Chips (Weis) – Incorrect Sodium Claims (2014)

Firm's sodium claims of 55 g/serving is incorrect. Product analyzed and found to contain shows approx. 290 mg/serving size

Class IIILow

FDADec 16, 2014CT, ME, MA +5 more• Keystone Food Products Inc

Volkswagen Jetta (VOLKSWAGEN) – headlight defect (2014)

Volkswagen Group of America, Inc. (Volkswagen) is recalling certain model year 2015 Jetta vehicles manufactured July 11, 2014, to November 13, 2014. Due to incorrect software within the headlight control module, the low beam headlights may turn off when high beam lights are turned on. As a result, the light output from the headlights may be insufficient. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) No. 108. "Lamps, Reflective Devices, and Associated Equipment."

NHTSADec 15, 2014Nationwide• VOLKSWAGEN

Lactate Assay (Beckman Coulter) – interference risk (2014)

N-Acetyl Cysteine (NAC), when administered in therapeutic concentrations for the treatment of acetaminophen overdose, interferes with the assays for these analytes: Cholesterol OSR6X16, Uric Acid OSR6X98, Lactate OSR6X93, and Lipase OSR6X30. NAC interference may lead to falsely low results.

Class IIModerate

FDADec 15, 2014Nationwide• Beckman Coulter Inc.

Lipase Assay (Beckman Coulter) – interference risk (2014)

Class IIModerate

FDADec 15, 2014Nationwide• Beckman Coulter Inc.

Trident PSL HA Solid Back (Stryker) – Manufacturing Complaint (2014)

Five customer complaints were received for the same batch of Trident PSL Shells (part number 540-11-50E lot 49073501) alleging that when the packages were opened there were no dome holes plugs present.

Class IIModerate

FDADec 15, 2014Nationwide• Stryker Howmedica Osteonics Corp.