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Applied Medical Resources Recalls
30 recalls on record · October 3, 2012 to January 14, 2026 · 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.
January 14, 2026Medical DevicesFDA
Applied Medical Resources Corp recalls Kii Low Profile, Bladed Dual Pack , Qty. 1 5x55mm REF: CTB23
Hazard: There is the potential for extended length of the blade obturator after assembly into the cannula and seal housing.
April 3, 2024Medical DevicesFDA
Applied Medical Resources Corp recalls Epix Universal Clip Applier, REF: CA500, STERILEEO included within the following kit Reference Numbers: GK1003, AME Kit
Hazard: Their is the potential that Universal Clip applier may not load clip after the trigger is actuated.
April 3, 2024Medical DevicesFDA
Applied Medical Resources Corp recalls Epix Universal Clip Applier, REF: CA500, STERILEEO
Hazard: Their is the potential that Universal Clip applier may not load clip after the trigger is actuated.
June 3, 2020Medical DevicesFDA
Applied Medical Resources Corp recalls Clip Applier Kit, REF: K2887, UDI: (01)30607915139132(17)220822(30)1(10)
Hazard: There may be a slightly protruding rivet on the distal end of the laparoscopic grasper which has the potential for tissue to catch on it during use and lead to tissue damage.
June 3, 2020Medical DevicesFDA
Applied Medical Resources Corp recalls DR. THAMES - LAP CHOLE, REF: K0880, UDI: (01)30607915139620
Hazard: There may be a slightly protruding rivet on the distal end of the laparoscopic grasper which has the potential for tissue to catch on it during use and lead to tissue damage.
June 3, 2020Medical DevicesFDA
Applied Medical Resources Corp recalls Epix latis GRASPER, 5mm x 45 cm, REF: C4140, Qty: 10, Sterile R, CE, Rx ONLY, UDI: (01)00607915110154
Hazard: There may be a slightly protruding rivet on the distal end of the laparoscopic grasper which has the potential for tissue to catch on it during use and lead to tissue damage.
June 3, 2020Medical DevicesFDA
Applied Medical Resources Corp recalls Epix latis GRASPER, 5 mm x 35 cm, REF C4130, Qty: 10, Sterile R, CE, Rx ONLY, UDI: (01)00607915110147
Hazard: There may be a slightly protruding rivet on the distal end of the laparoscopic grasper which has the potential for tissue to catch on it during use and lead to tissue damage.
May 27, 2020Medical DevicesFDA
Applied Medical Resources Corp recalls STEALTH SPRING CLIP 6mm latis (1/4 Force). Non-Sterile, REF/UDI::A1702/(01)10607915110649 - Product Usage: The device is
Hazard: Failure of cardiovascular clips to provide sufficient occlusion of the vessel.
May 27, 2020Medical DevicesFDA
Applied Medical Resources Corp recalls STEALTH SPRING CLIP 6mm latis (3/4 Force). REF/UDI::A1603/(01)00607915110581 - Product Usage: The device is indicated fo
Hazard: Failure of cardiovascular clips to provide sufficient occlusion of the vessel.
May 27, 2020Medical DevicesFDA
Applied Medical Resources Corp recalls STEALTH SPRING CLIP 6mm latis (1/4 Force). REF/UDI::A1602/(01)00607915110574 - Product Usage: The device is indicated fo
Hazard: Failure of cardiovascular clips to provide sufficient occlusion of the vessel.
May 27, 2020Medical DevicesFDA
Applied Medical Resources Corp recalls STEALTH SPRING CLIP 6mm latis (1/2 Force). REF/UDI::A1601/(01)00607915110567 - Product Usage: The device is indicated fo
Hazard: Failure of cardiovascular clips to provide sufficient occlusion of the vessel.
May 13, 2020Medical DevicesFDA
Applied Medical Resources Corp recalls Applied Medical Dual Lumen Graft Cleaning Catheter & 1cc SYRINGE Nonpyrogenic, REF: A4GW6, 5F X 60cm, 9mm, Sterile EO, C
Hazard: The firm has received reports of tip separation during usage of the catheters, which may expose patients to unintended dislodgement of the tip from the body of the catheter.
May 13, 2020Medical DevicesFDA
Applied Medical Resources Corp recalls Bard Embolectomy Catheter & 1 ml SYRINGE, REF numbers/UDI: CE0340DR/(01)H699CE0340DR10R; CE0380DR/(01)H699CE0380DR10
Hazard: The firm has received reports of tip separation during usage of the catheters, which may expose patients to unintended dislodgement of the tip from the body of the catheter.
May 13, 2020Medical DevicesFDA
Applied Medical Resources Corp recalls Python Embolectomy Catheters, Sterile EO, CE, Ref numbers/UDI: A4E01/(01)00607915113407; A4E02/(01)00607915113414; A4E
Hazard: The firm has received reports of tip separation during usage of the catheters, which may expose patients to unintended dislodgement of the tip from the body of the catheter.
November 27, 2019Medical DevicesFDA
Applied Medical Resources Corp recalls GelPOINT Path Transanal Procedural Pack with Epix Electrosurgical L-Hook with Smoke Evacuation, 4x5.5cm and 5mm x 42cm
Hazard: Unintentional shifting of the tip insulation of the firm's electrosurgical probes.
November 27, 2019Medical DevicesFDA
Applied Medical Resources Corp recalls Epix Electrosurgical Probes with Smoke Evacuation, Angled L-Hook Tip, 5mm x 42 cm REF CW002 QTY: 1 - Product Usage:
Hazard: Unintentional shifting of the tip insulation of the firm's electrosurgical probes.
July 17, 2019Medical DevicesFDA
Applied Medical Resources Corp recalls Kii Fios First Entry, 5 X 75 mm, RX only, REF CFF05 Qty: 6, Sterile R, Lot: 1330981, Exp: July 15, 2021, Applied Medica
Hazard: The product may not have met sterility requirements . Use of a non-sterile device on a patient may expose the patient to infectious agents.
June 21, 2017Medical DevicesFDA
Applied Medical Resources Corp recalls Kii Shielded Bladed trocars (CTB14), Kii Low profile trocars (CTB23), and Kii 5x55mm Optical Z-Thread Dual Pack (CTR14
Hazard: Due to possibility of insufficient sterilization.
May 18, 2016Medical DevicesFDA
Applied Medical Resources Corp recalls Direct Drive Clip Applier CA090, indicated for ligation of tubular structures or vessels in laparoscopic and general sur
Hazard: Increased customer complaints indicating inconsistent clip application; may lead to unoccluded vessels.
April 13, 2016Medical DevicesFDA
Applied Medical Resources Corp recalls STD KIT GK260, Standard Set 360 Z Product Usage: The Epix disposable laparoscopic clip applier is indicated for lig
Hazard: Applied Medical Resources Corporation is recalling CA500 Epix Universal Clip Applier, kit models STD GK258 AME Standard Kit 44, STD KIT GK213, AME Standard Kit 15, and STD KIT GK260, Standard Set 360 Z, which contain the affected CA500 lot, because of a potential loading mechanism nonconformance.
April 13, 2016Medical DevicesFDA
Applied Medical Resources Corp recalls STD KIT GK213, AME Standard Kit 15 Product Usage: The Epix disposable laparoscopic clip applier is indicated for li
Hazard: Applied Medical Resources Corporation is recalling CA500 Epix Universal Clip Applier, kit models STD GK258 AME Standard Kit 44, STD KIT GK213, AME Standard Kit 15, and STD KIT GK260, Standard Set 360 Z, which contain the affected CA500 lot, because of a potential loading mechanism nonconformance.
April 13, 2016Medical DevicesFDA
Applied Medical Resources Corp recalls STD GK258, AME Standard Kit 44 Product Usage: The Epix disposable laparoscopic clip applier is indicated for ligati
Hazard: Applied Medical Resources Corporation is recalling CA500 Epix Universal Clip Applier, kit models STD GK258 AME Standard Kit 44, STD KIT GK213, AME Standard Kit 15, and STD KIT GK260, Standard Set 360 Z, which contain the affected CA500 lot, because of a potential loading mechanism nonconformance.
April 13, 2016Medical DevicesFDA
Applied Medical Resources Corp recalls CA500 Epix Universal Clip Applier Product Usage: The Epix disposable laparoscopic clip applier is indicated for lig
Hazard: Applied Medical Resources Corporation is recalling CA500 Epix Universal Clip Applier, kit models STD GK258 AME Standard Kit 44, STD KIT GK213, AME Standard Kit 15, and STD KIT GK260, Standard Set 360 Z, which contain the affected CA500 lot, because of a potential loading mechanism nonconformance.
September 23, 2015Medical DevicesFDA
Applied Medical Resources Corp recalls Voyant Open Fusion Device Models: EB040 and EB040+ Product Usage: The Applied Voyant Open Fusion Device is designed
Hazard: Potential to improperly characterize tissue within the jaws, which may result in nonoptimal power delivery.
November 20, 2013Medical DevicesFDA
Applied Medical Resources Corp recalls Applied Medical's Inzii¿ 12/15mm Retrieval System. Applieds Inzii Tissue Retrieval Bag, Model Number CD004, is class
Hazard: Applied Medical is conducting a voluntary recall of the Inzii¿ 12/15mm retrieval system. During shipment, the retrieval system packaging has the potential to become punctured with small holes, which could compromise the sterile barrier. The likelihood of this situation to occur and result in patient harm is highly unlikely; however, out of an abundance of caution for patient safety and a commitmen
June 19, 2013Medical DevicesFDA
Applied Medical Resources Corp recalls Applied Medicals Epix¿ and Direct Drive Laparoscopic Graspers, Model Numbers C4130 and C4140. Used for grasping and
Hazard: Applied Medical is conducting a voluntary recall on specific lot numbers of its Epix¿ and Direct Drive Laparoscopic Graspers. When the ratchet trigger is activated, if a great enough force is applied, there is a potential for the trigger to fracture and the jaws to remain in the closed position. The likelihood of this situation to occur and result in permanent patient injury is highly unlikely;
January 16, 2013Medical DevicesFDA
Applied Medical Resources Corp recalls Laparoscope, general; plastic surgery Used for general, abdominal, gynecological and thoracic minimally invasive surg
Hazard: Applied Medical is conducting a voluntary recall on a specific lot number of its 12x150mm Kii shielded bladed access systems. This is due to a potential for the blade to remain exposed after shield deployment. Further use of any affected product should cease immediately. The affected model number is CTB71, and the affected lot is 1179107.
October 3, 2012Medical DevicesFDA
Applied Medical Resources Corp recalls Irrigation Catheters (Models IRR-XXX-XX): Model Numbers & Description: IRR-023-10F,CATHETER IRRIGATION 10F 23CM; IR
Hazard: Applied Medical is recalling specific lot numbers of its Vascular Catheters because they may have a potential for packaging particulate matter to reside on the product.
October 3, 2012Medical DevicesFDA
Applied Medical Resources Corp recalls Biliary Catheters (Models A47XX and CB0XXXXX): Model Numbers & Description: A4752, SYNTEL BILIARY 5F-23CM CATHETER;
Hazard: Applied Medical is recalling specific lot numbers of its Vascular Catheters because they may have a potential for packaging particulate matter to reside on the product.
October 3, 2012Medical DevicesFDA
Applied Medical Resources Corp recalls Embolectomy Catheters (Models A44XX, A4FXX, CE0XXXST, and CE0XXX): Model Numbers & Description: A4402, 3F-40CM, SYNT
Hazard: Applied Medical is recalling specific lot numbers of its Vascular Catheters because they may have a potential for packaging particulate matter to reside on the product.