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Sources: EU EUDAMED, US FDA
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FDA Recall
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Zimmer Air Dermatome, Model/Catalog Number: 00880100100
FDA Recall
Open, Classified
·Zimmer Surgical Inc·Product code GFD·November 24, 2025
Caphosol Artificial Saliva (32 doses sachet box). 64 x 15 mL sachets aqueous solution (32 sachets Solution A Phosphate, 32 sachets Solution B Calcium)
FDA Recall
Open, Classified
·RECORDATI RARE DISEASES INC.·Product code LFD·June 11, 2025
Integra Padgett Dermatome Set - Product Usage: are intended for use in the cutting of skin grafts for use in plastic surgery and/or burn treatment. These instruments are intended only for professional use in hospitals and similar medical facilities, where the patient will be under the supervision of trained personnel.
FDA Recall
Terminated
·Integra LifeSciences Corp.·Product code GFD·August 4, 2020
Zimmer Air Dermatome II, REF 00-8851-001-00 handpiece Rx, non-sterile grafting instruments intended to provide variable graft thickness and width capabilities
FDA Recall
Terminated
·Zimmer Surgical Inc·Product code GFD·May 7, 2013
Zimmer Air Dermatome II, REF 00-8851-001-01 handpiece, w/o hose, Rx, non-sterile grafting instruments intended to provide variable graft thickness and width capabilities.
FDA Recall
Terminated
·Zimmer Surgical Inc·Product code GFD·May 7, 2013
Zimmer Air Dermatome II Handpiece Loaner, item number 01-8851-001-00. Device is packaged inside of a padded-foam corrugate box. A product label is applied to the lid of the box. The width plates, when sold individually, are placed in a labeled poly zipper bag, which is then placed into a corrugated shipper carton or padded envelope.
FDA Recall
Terminated
·Zimmer Surgical Inc·Product code GFD·July 4, 2016
Amalgatome SD, COAXIAL PNEUMATIC HOSE, SCHRADER, Model X101004
FDA Recall
Terminated
·Exsurco Medical·Product code GFD·April 17, 2018
Zimmer Dermatome Blades- 10-pack boxes of blades. Intended for use with the dermatome handpiece which is a skin grafting instrument that is intended to provide variable graft thickness and width capabilities Part number: 00880000010
FDA Recall
Open, Classified
·Zimmer Surgical Inc·Product code GFD·September 5, 2023
13 ft Handpiece Cable, component of the Dermatome Sets Model S and Model S6 and also as a spare part - Product Usage: are intended for use in the cutting of skin grafts for use in plastic surgery and/or burn treatment. These instruments are intended only for professional use in hospitals and similar medical facilities, where the patient will be under the supervision of trained personnel.
FDA Recall
Terminated
·Integra LifeSciences Corp.·Product code GFD·August 4, 2020
Zimmer Air Dermatome II Width Plate, 4 inch. Part #00-8851-204-00. Width plate is packaged inside of a padded-foam corrugate box. A product label is applied to the lid of the box. The width plates, when sold individually, are placed in a labeled poly zipper bag, which is then placed into a corrugated shipper carton or padded envelope. The Zimmer Air Dermatome II is a skin grafting instrument that is intended to provide variable graft thickness and width capabilities.
FDA Recall
Terminated
·Zimmer Surgical Inc·Product code GFD·July 4, 2016
Zimmer Dermatone AN, Model No. 88710100
FDA Recall
Terminated
·Zimmer Surgical Inc·Product code GFD·June 8, 2018
SUNSTAR G.U.M. HYDRAL DRY MOUTH RELIEF On-the-go Oral Spray, 2 FL.OZ. UPC0 70942 30713 0 - Product Usage: The device is formulated with water, moisturizers /humectants including one plant-based moisture rich humectant, sweeteners and flavors that collectively have lubricating, moisturizing, soothing, and refreshing properties to help relieve and manage the symptoms of dry mouth.
FDA Recall
Terminated
·Sunstar Americas, Inc.·Product code LFD·February 18, 2021
Biotene Moisturizing Mouth Spray, with xylitol, For dry mouth symptom relief, 44.3ml/1.5 FL. OZ., Sugar Free Sweetened with xylitol and sorbitol, GlaxoSmithKline, Consumer Healthcare, L.P., Moon Township, PA 15108. Biotene Mouth Spray is used for the treatment of dry mouth
FDA Recall
Terminated
·GlaxoSmithKline, LLC.·Product code LFD·October 17, 2013
Zimmer Dermatome AN, Model/Catalog Number: 88710100
FDA Recall
Open, Classified
·Zimmer Surgical Inc·Product code GFD·November 24, 2025
CelluTome Epidermal Harvesting System Part number CT-H25 or Part Number CT-H50
FDA Recall
Terminated
·KCI USA, Inc.·Product code GFD·May 19, 2014
Moi-Stir oral swabsticks, an aid to mouth care and oral hygiene, CONTENTS: 3 fibre-tipped swabsticks premoistened with MOI-STIR mouth moistening solutioon and saliva supplement; Product Nos. 55299-703-03 and 55299-703-25. Distributed by Kingswood Laboratories, Inc., Indianapolis, IN 46256-3316. Swabs are sold only in case quantities of 25 foil packs to the carton and 100 foil packs to the case.
FDA Recall
Terminated
·Kingswood Laboratories, Inc·Product code LFD·April 22, 2005
Zimmer Air Dermatome II Width Plate, 2 inch. Part # 885120200. Width plate is packaged inside of a padded-foam corrugate box. A product label is applied to the lid of the box. The width plates, when sold individually, are placed in a labeled poly zipper bag, which is then placed into a corrugated shipper carton or padded envelope. The Zimmer Air Dermatome II is a skin grafting instrument that is intended to provide variable graft thickness and width capabilities.
FDA Recall
Terminated
·Zimmer Surgical Inc·Product code GFD·July 4, 2016
Zimmer Air Dermatome II Width Plate, 1.5 inch. Part #00-8851-215-00. Width plate is packaged inside of a padded-foam corrugate box. A product label is applied to the lid of the box. The width plates, when sold individually, are placed in a labeled poly zipper bag, which is then placed into a corrugated shipper carton or padded envelope. The Zimmer Air Dermatome II is a skin grafting instrument that is intended to provide variable graft thickness and width capabilities.
FDA Recall
Terminated
·Zimmer Surgical Inc·Product code GFD·July 4, 2016
Universal Power Supply Units, Part Number DP0007 and DP0800 , for use with the Integra Padgett Dermatomes - Model S, SB, and S6, Device Listing #E208841, 510 (k) exempt. The Integra Padgett Dermatomes are intended for use in the cutting of skin grafts for use in plastic surgery and/or burn treatment. The Model S and S6 dermatomes are intended for professional use in hospitals, and similar medical facilities, where the patient will be under the supervision of trained personnel. The Model SB dermatomes are used in skin banks for the harvesting of cadaver tissues.
FDA Recall
Terminated
·Integra LifeSciences Corp.·Product code GFD·March 11, 2011
Wallace Artificial Insemination Catheter, 180 mm, Sterile, Quantity: 1 Box (10 units), Model: AIC18JP, Cooper Surgical Inc., (01) 2 0888937 021749 - Product Usage: Intended use of the product is the introduction of washed spermatozoa into the uterine cavity.
FDA Recall
Terminated
·CooperSurgical, Inc.·Product code MFD·February 28, 2020