Zimmer Recalls
1030 recalls on record in the United States
Zimmer GmbH recalls Normed Charcot Osteotome Chisel (Various sizes)
Product may contain a gap between the handle and metal chisel which can lead to failure to properly disinfect or sterilize between use.
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Zimmer Biomet, Inc. recalls A.L.P.S. MIS Calcaneus Locking Plate LG RT F.A.S.T. Guide in
The drill guides were manufactured with the incorrect color anodization.
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Zimmer Biomet, Inc. recalls AIM Tibial Nails intramedullary fixation rod - NON-STERILE;
The AIM Tibial Nails failed a clinical analysis where the surgical revision rate exceeded the acceptance criteria in the Device Performance Review protocol for the implant system.
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Zimmer Biomet, Inc. recalls ACE Trochanteric Nail System STER TROC NAIL 180X11X140 STE
Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric Nail (ATN) system after a Device Performance Review (DPR) failed clinical analysis for survivorship pursuant to the acceptance criteria for the DPR protocol for the ATN system.
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Zimmer Biomet, Inc. recalls Zimmer M/L Taper Hip Prosthesis, 7711 Series, Femoral Stem 1
Certain packages labeled as size 7.5 Extended Offset Reduced Neck length hip implant, actually contained a Size 4 Standard Reduced Neck length taper hip implant.
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Zimmer Biomet, Inc. recalls Persona Partial Knee spacer block instruments; (1) 8mm block
Certain partial knee implant spacer blocks do not fit in the alignment tower instrument or handle.
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Zimmer Biomet, Inc. recalls ACE Trochanteric Nail System STER TROC LAG SCR 70 MM The
Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric Nail (ATN) system after a Device Performance Review (DPR) failed clinical analysis for survivorship pursuant to the acceptance criteria for the DPR protocol for the ATN system.
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Zimmer Biomet, Inc. recalls ACE Trochanteric Nail System ACE TROCH NAIL 125 DEG. X 11MM
Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric Nail (ATN) system after a Device Performance Review (DPR) failed clinical analysis for survivorship pursuant to the acceptance criteria for the DPR protocol for the ATN system.
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Zimmer Biomet, Inc. recalls ACE Trochanteric Nail System STER L H TROC NAIL 320X9X125
Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric Nail (ATN) system after a Device Performance Review (DPR) failed clinical analysis for survivorship pursuant to the acceptance criteria for the DPR protocol for the ATN system.
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Zimmer Biomet, Inc. recalls Zimmer M/L Taper Hip Prosthesis, 7711 Series, Femoral Stem 1
Certain packages labeled as size 7.5 Extended Offset Reduced Neck length hip implant, actually contained a Size 4 Standard Reduced Neck length taper hip implant.
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Zimmer Biomet, Inc. recalls ACE Trochanteric Nail System STER TROC NAIL 180X13X140 STE
Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric Nail (ATN) system after a Device Performance Review (DPR) failed clinical analysis for survivorship pursuant to the acceptance criteria for the DPR protocol for the ATN system.
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Zimmer Biomet, Inc. recalls ACE Trochanteric Nail System TROCH NAIL ST 13X180 125DG STR
Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric Nail (ATN) system after a Device Performance Review (DPR) failed clinical analysis for survivorship pursuant to the acceptance criteria for the DPR protocol for the ATN system.
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Zimmer Biomet, Inc. recalls AIM Tibial Nails intramedullary fixation rod - STERILE; Item
The AIM Tibial Nails failed a clinical analysis where the surgical revision rate exceeded the acceptance criteria in the Device Performance Review protocol for the implant system.
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Zimmer Biomet, Inc. recalls ACE Trochanteric Nail System ATN LAG SCREW 60MM STERILE AT
Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric Nail (ATN) system after a Device Performance Review (DPR) failed clinical analysis for survivorship pursuant to the acceptance criteria for the DPR protocol for the ATN system.
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Zimmer Biomet, Inc. recalls Coonrad/Morrey Elbow Implant System humeral assembly 4IN XSM
One lot of humeral stem implants do not include the humeral bushing components.
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Zimmer Biomet, Inc. recalls ACE Trochanteric Nail System STER TROC END CAP STER TROC E
Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric Nail (ATN) system after a Device Performance Review (DPR) failed clinical analysis for survivorship pursuant to the acceptance criteria for the DPR protocol for the ATN system.
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Zimmer Dental Inc recalls Tapered Screw-Vent MTX, Dental Implant, sterile. Model TSVT
Two lots of the Tapered Screw-Vent Implants, with different outer thread diameters, were inadvertently commingled during the manufacturing process and may be mislabeled.
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Zimmer Biomet, Inc. recalls ACE Trochanteric Nail System STER TROC NAIL 125 DEG X 9MM
Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric Nail (ATN) system after a Device Performance Review (DPR) failed clinical analysis for survivorship pursuant to the acceptance criteria for the DPR protocol for the ATN system.
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Zimmer Biomet, Inc. recalls Persona Partial Knee Spacer Blocks To assist in partial k
Zimmer Biomet is conducting a medical device recall for the Persona Partial Knee Spacer Blocks in sizes 8mm, 9mm, 10mm, 12mm, and 14mm. Complaints received indicated that flexion has the potential to feel tight during range-of-motion trialing and that the final trial has the potential to appear looser in extension.
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Zimmer Biomet, Inc. recalls PERSONA¿ THE PERSONALIZED KNEE SYSTEM "PSN TIB STM 5 DEG SZ
A complaint was received for Item 42-5320-067-02, lot 63236047. It was report that there was no set screw or taper plug included in the box. Complaint investigation confirmed that the entire lot of 63236047 was missing the set screw and taper plug.
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Zimmer Biomet, Inc. recalls Phoenix Nail System, intended for use with an intramedullary
Certain lots of the Phoenix Tibia Nail 3.5mm Inserter instruments are being recalled due to reports of fracturing and remaining in the device implant.
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Zimmer Dental Inc recalls Tapered Screw-Vent MTX, Dental Implant, sterile. Model TSV4
Two lots of the Tapered Screw-Vent Implants, with different outer thread diameters, were inadvertently commingled during the manufacturing process and may be mislabeled.
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Zimmer Biomet, Inc. recalls ACE Trochanteric Nail System ATN AR SCREW 60MM STERILE ATN
Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric Nail (ATN) system after a Device Performance Review (DPR) failed clinical analysis for survivorship pursuant to the acceptance criteria for the DPR protocol for the ATN system.
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Zimmer Biomet, Inc. recalls ACE Trochanteric Nail System TROCH NAIL ST 11X180 125DG STR
Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric Nail (ATN) system after a Device Performance Review (DPR) failed clinical analysis for survivorship pursuant to the acceptance criteria for the DPR protocol for the ATN system.
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Zimmer Biomet, Inc. recalls CPT 12/14 COCR SIZE 0 STD prosthesis, hip, semi-constrai
The LDPE bag packaging for various highly polished hip and knee implants may adhere to the highly polished surface, leaving residue or material from the LDPE bag on the implant after it is removed from the bag.
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Zimmer Biomet, Inc. recalls VERSYS 6 INCH BEADED FC 13X160MM LM BODY EXT NECK & STD NECK
The LDPE bag packaging for various highly polished hip and knee implants may adhere to the highly polished surface, leaving residue or material from the LDPE bag on the implant after it is removed from the bag.
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Zimmer Biomet, Inc. recalls LPS PRECOAT FEM SIZE D-RT LPS PRECOAT FEM SIZE E-RT LPS PO
The LDPE bag packaging for various highly polished hip and knee implants may adhere to the highly polished surface, leaving residue or material from the LDPE bag on the implant after it is removed from the bag.
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Zimmer Biomet, Inc. recalls CR OPTION FEM COMP SIZE C/L CR OPTION FEM COMP SIZE C/R CR
The LDPE bag packaging for various highly polished hip and knee implants may adhere to the highly polished surface, leaving residue or material from the LDPE bag on the implant after it is removed from the bag.
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Zimmer Biomet, Inc. recalls LPS-FLEX OPTION FEMORAL C-L LPS-FLEX OPTION FEMORAL C-L LP
The LDPE bag packaging for various highly polished hip and knee implants may adhere to the highly polished surface, leaving residue or material from the LDPE bag on the implant after it is removed from the bag.
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Zimmer Biomet, Inc. recalls CR-FLEX POR HATCP FEM C-L CR-FLEX POR HATCP FEM C-R CR-FLE
The LDPE bag packaging for various highly polished hip and knee implants may adhere to the highly polished surface, leaving residue or material from the LDPE bag on the implant after it is removed from the bag.
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Showing 30 of 1030 recalls. See all →