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Cypress Medical Products Recalls
11 recalls on record · May 15, 2013 to September 25, 2024 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
September 25, 2024Medical DevicesFDA
Cypress Medical Products LLC recalls Acceava Respiratory Strep A, CLIA Waived, Catalog Number 4580295008
Hazard: Due to a classification error in our inventory management system, these medical devices were shipped to customers that did not have the requisite license to purchase such devices.
September 25, 2024Medical DevicesFDA
Cypress Medical Products LLC recalls BinaxNOW Respiratory Strep A Test Kit, CLIA Waived, Catalog Number 730025
Hazard: Due to a classification error in our inventory management system, these medical devices were shipped to customers that did not have the requisite license to purchase such devices.
September 25, 2024Medical DevicesFDA
Cypress Medical Products LLC recalls General Purpose Syringe McKesson 60 mL Luer Lock Tip Without Safety, Catalog Number 869662, McKesson Brand Catalog Numbe
Hazard: The syringes that were inadvertently shipped from the Distribution Center. This product was on quarantine because FDA has stated that these syringes lack FDA clearance and were inadvertently shipped due to an internal order processing error.
September 4, 2024Medical DevicesFDA
Cypress Medical Products LLC recalls McKesson Syringe 60CC, Luer Lock Tip, Sterile, ITEM NO 102-S60C. Model No. 102-S60C - SYRINGE, LL 60CC (25/BX 4BX/CS)
Hazard: Affected syringes lack FDA clearance.
September 22, 2021Medical DevicesFDA
Cypress Medical Products LLC recalls McKesson Lap Sponge, X-Ray Detectable 12"x 12", 5/pack, Sterile McKesson Part # 16-2112121
Hazard: Manufacturer issued a recall due to an EO indicator color. The indicator should change from red to blue signifying sterilization. However, on one case of product, the indicators did not change
April 10, 2019Medical DevicesFDA
Cypress Medical Products LLC recalls McKesson Consult Diagnostic Immunochemical Fecal Occult Blood Test, Part numbers 178-CK30T, 178-CT30, 178¿TBSO, 178-CM25
Hazard: Products were denied Clinical Laboratory Improvement Amendments (CLIA) waiver approval by the FDA, due to the packaging being too similar to domestically sourced products under the same branded label.
October 24, 2018Medical DevicesFDA
Cypress Medical Products LLC recalls McKesson Insulin Syringe 0.3mL 31GX5/16 Item Numbers: 102-SN310C31516P Product Usage: Indication of Use: Injection
Hazard: Small hole at the end of the syringe is impeding suction of liquid.
August 22, 2018Medical DevicesFDA
Cypress Medical Products LLC recalls Powder Free Vinyl Exam Gloves, Item Nos. 14-116, 14-118 Product Usage: Medical exam glove for use by professional he
Hazard: The firm is recalling one lot of McKesson Powder Free Vinyl Exam Gloves because a sample of product from that lot did not meet certain release specifications. It is possible that certain gloves from this lot may not be of medical exam quality and, therefore, may not provide an effective barrier to infectious material.
March 14, 2018Medical DevicesFDA
Cypress Medical Products LLC recalls 241-McKesson Premium Skin Staple Remover Kit, Item #100123, McKesson I.V. Start Kit, 100124-McKesson Suture Removal Kit,
Hazard: Product not meeting the iodine assay level requirements to support 36 month expiration dating.
December 21, 2016Medical DevicesFDA
CYPRESS MEDICAL PRODUCTS recalls McKesson Powder Free Vinyl Exam Gloves Catalog numbers 14-116, 14-118, 14-120, 14-136, 14-138 and 14-140
Hazard: A container of McKesson vinyl gloves that failed the FDA leak test was inadvertently distributed.
May 15, 2013Medical DevicesFDA
Cypress Medical Products LLC recalls Cypress Medical Products LLC, MediChoice Umbilical cord clamp, sterile; single use; Distributed by Owens & Minor, Mech
Hazard: Cypress Medical Products LLC is voluntarily recalling one lot of the Owens and Minor (O&M) Umbilical Cord Clamps because recent complaints indicate the clamps are breaking upon use. The product may not perform as intended.