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FDA (Device enforcement)Recalled 2016-11-08closedclass ii

Stryker Medical Division of Stryker Corporation: Performance-LOAD Ambulance Cot Fastener Stretcher, Wheeled

Is my product affected?

Performance-LOAD Ambulance Cot Fastener Stretcher, Wheeled

  • UPC 07613327282542
  • UPC 07613327282603
  • UPC 07613327282597
  • UPC 07613327282610

Check against the official notice below — it lists the full affected range.

What happened

Stryker Medical voluntarily recalled 749 Performance-LOAD Cot Fasteners due to reports that the fastening system may not secure properly or fasten into the Performance-LOAD equipment. In some cases, the fastener bounced back during loading, which could potentially cause injury. The affected fasteners were distributed worldwide, including to all U.S. states, Canada, and the Netherlands. The recalled models are 6392-000-001, 6392-000-002, 6393-000-003, and 6393-000-004.

The source document does not specify what affected consumers should do regarding this recall.

Written by software from the official notice below. Not reviewed by a lawyer.

Hazard

Stryker Medical initiated a voluntary recall of Stryker Performance-LOAD Cot Fasteners due to complaints that fastening system may not have been securely fastened or had an inability to fasten into the Performance-LOAD and bounced back during loading which could cause injury to consumers.

Details from the source

Reason for recall: Stryker Medical initiated a voluntary recall of Stryker Performance-LOAD Cot Fasteners due to complaints that fastening system may not have been securely fastened or had an inability to fasten into the Performance-LOAD and bounced back during loading which could cause injury to consumers. Distribution: Worldwide Distribution to AK, AL , AR , AZ , CA , CT , DC , DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NY, OH, OK, OR, PA , RI, SC, TN, TX, UT,VA, VT ,WA ,WV ,WY and Internationally to Canada and the Netherlands Quantity: 749 units Lot/code info: Model(s): 6392-000-001, 6392-000-002, 6393-000-003, 6393-000-004; GTIN: 07613327282542, 07613327282603, 07613327282597, 07613327282610

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.

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