Skeletal Kinetics, Llc: 20 recalls on record

Recalls filed with 1 agency: FDA (20).

First recall on record: May 27, 2020. Most recent: July 22, 2020.

Risk classification: Class II: 20

Most recent recalls

DateAgencyProduct
July 22, 2020FDACRANIOSCULPT FLOW, 3CC. Product Number: C-FLOW3CC, UDI: 813845020320 - - Product Usage: …Z-2600-2020
July 22, 2020FDACRANIOSCULPT, CMF IMPACT, 3CC Product Number: C-CMF3CC, UDI: 813845020931 - Product Usag…Z-2633-2020
July 22, 2020FDAACUMED CALLOS INJECT 5CC. Product Number: 65-0005-S, UDI: 813845020238 - Product Usage: …Z-2594-2020
July 22, 2020FDAEXACTECH OSSILIX FIL (MX), 5CC. Product Number: 660-02-05, UDI: 813845021006 - Product U…Z-2607-2020
July 22, 2020FDAOSTEOVATIONEX 5CC, INJECT FORMULA. Product Number: 390-0005, UDI: 813845020023 - Product…Z-2622-2020
July 22, 2020FDAOSTEOVATION, 5CC, IMPACT FORMULA. Product Number: 390-2105, UDI: 813845020085 - Product …Z-2619-2020
July 22, 2020FDACRANIOSCULPT FLOW, OUS, 10CC. Product Number: C-FLOW10CC-OUS, UDI: 813845020382 - Produc…Z-2603-2020
July 22, 2020FDASKAFFOLD CMF IMPRESS (MP), 10CC. Product Number: CMMP-IM10, UDI: 813845020696 - Product …Z-2625-2020
July 22, 2020FDASKAFFOLD FLOW, 10CC. Product Number: SKMX-FL10, UDI: 813845020900 - Product Usage: Callo…Z-2629-2020
July 22, 2020FDASKAFFOLD FLOW (MX) 5CC. Product Number: SKMX-FL05, UDI: 813845020894 - Product Usage: Ca…Z-2628-2020
July 22, 2020FDAEXACTECH OSSILIX MP FIL, 10CC. Product Number: 662-02-10, UDI: 813845021051 - Product Us…Z-2636-2020
July 22, 2020FDAMEDTRONIC BONE VOID FILLER, LARGE. Product Number: C07B, UDI: 813845020511 - Product Usa…Z-2610-2020
July 22, 2020FDAOSTEOVATION IMPACT 10CC and OSTEOVATION, 10CC, IMPACT FORMULA, Product Number: 390-2110, …Z-2614-2020
July 22, 2020FDAEXACTECH OSSILIX FIL (MX), 10CC. Product Number: 660-02-10, UDI: 813845021013 - - Produc…Z-2606-2020
July 22, 2020FDACRANIOSCULPT FLOW, CAN, 5CC. Product Number: C-FLOW5CC-CAN, UDI: 813845020344 - Product …Z-2602-2020
July 22, 2020FDAOSTEOVATION EX, 5CC, IMPACT FORMULA. Product Number: 390-0205, UDI: 813845020047 - Produ…Z-2613-2020
July 22, 2020FDACRANIOSCULPT FLOW, CAN, 10CC, Product Number: C-FLOW10CC-CAN, UDI: 813845020375 - Produc…Z-2632-2020
July 22, 2020FDACRANIOSCULPT, CMF IMPACT, 10CC, Product Number: C-CMF10CC, UDI: 813845020955 - Product U…Z-2635-2020
July 22, 2020FDAOSTEOVATION RMX 10CC. Product Number: 390-6002, UDI: 813845021099 - Product Usage: Callo…Z-2615-2020
May 27, 2020FDACranio/Sculpt C, 10cc, Bone Void Filler, UDI: 00813845021129 - Product Usage: CRANIO/SCUL…Z-2054-2020

Questions about this company

How many recalls does Skeletal Kinetics, Llc have?
Recalert has 20 U.S. recalls on record for Skeletal Kinetics, Llc, published between May 27, 2020 and July 22, 2020.
What was the most recent Skeletal Kinetics, Llc recall?
FDA recall Z-2600-2020, published July 22, 2020: CRANIOSCULPT FLOW, 3CC. Product Number: C-FLOW3CC, UDI: 813845020320 - - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal system (i.e. extremities, spine, pelvis). These…
Which agencies have handled Skeletal Kinetics, Llc recalls?
Skeletal Kinetics, Llc appears as the recalling firm in recalls from: FDA (20).

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