State

US Virgin Islands product recalls

73,833 recalls have nationwide distribution and so reach US Virgin Islands. 178 additional recalls listed US Virgin Islands specifically in their distribution scope.

What the numbers show

Total: 178
Critical: 12
Severe: 39
Most recent: 2026-10-21

Of the 178 recalls naming US Virgin Islands we have scored against our rubric, 12 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 39 (22%) are Severe.

Which agencies issued them

These figures cover only the 178 recalls whose distribution notice names US Virgin Islands specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

59376–59400 of 74011

ModerateFDA (Devices)·Z-1058-2014·2014-02-26
BioHorizons Recalls Dental Implants with Incorrect Length Labeling
BioHorizons is recalling 119 units of dental implants labeled as 10.5mm but actually measuring 12mm. The recall addresses a labeling error regarding the product's physical dimensions.
Product
External Implant RBT, D3 Threadform 4.0 X 10.5mm, REF 40105D3, STERILE R, Rx Only, BioHorizons(R), 2300 Riverchase Center, Birmingham, AL 35244 Usage: dental
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1032-2014·2014-02-26
Zimmer Recalls CPT 12/14 COCR Medical Devices Due to Packaging Validation Issues
Zimmer is recalling CPT 12/14 COCR devices because packaging operations at its Puerto Rico facility were not properly validated, despite passing seal integrity tests.
Product
CPT 12/14 COCR (various sizes)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1033-2014·2014-02-26
Zimmer Recalls 6 Degree Femoral Heads Due to Packaging Validation Issues
Zimmer is recalling 6 Degree COCR Femoral Heads and 6 Degree Unipolar Femoral Heads because packaging operations at a Puerto Rico facility were not properly validated.
Product
6 DEGREE COCR FEM HEAD (various sizes) and 6 DEG UNIPOLAR FEMORAL HE
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1041-2014·2014-02-26
Zimmer Recalls Self-Tapping Cortical Screws Due to Packaging Validation Issues
Zimmer, Inc. is recalling 7,044,680 self-tapping cortical screws because packaging operations at a Puerto Rico facility were not properly validated, raising concerns about sterile barrier integrity.
Product
2.7 X 6 CORT SCREW/SELFTA 2.7 X 7 CORT SCREW/SELFTA 2.7 X 8 CORT SCREW/SELFTA 2.7 X 9 CORT SCREW/SELFTA 2.7 X 10 CORT SCREW/SELFT 2.7 X 12 CORT SCREW/SELFT 2.7 X 14 CORT SCREW/SELFT 2.7 X 16 CORT SCREW/SELFT 2.7 X 18 CORT SCREW/SELFT 2.7 X 20 CORT SCREW/SELFT 2.7 X 22…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1015-2014·2014-02-26
Zimmer Recalls Orthopedic Implants Due to Packaging Validation Deficiencies
Zimmer is recalling specific orthopedic implants because packaging operations at its Puerto Rico facility were not properly validated, despite passing seal integrity tests.
Product
DISTAL MEDIAL FEMORAL CON, DISTAL POSTERIOR/LATERAL, DISTAL SMALL VOLAR RADIUS, PROXIMAL DORSAL ULNA PLT, and PROXIMAL MEDIAL TIBIAL 4.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1007-2014·2014-02-26
Zimmer Recalls M/DN R-F IM Nails Due to Packaging Validation Issues
Zimmer is recalling M/DN R-F IM Nails because packaging operations at its Puerto Rico facility were not properly validated, despite passing seal integrity tests.
Product
M/DN R-F IM NAIL 9MM DIA , 10 MM, 11 MM, 12 MM, 13 MM and 14 MM. Item codes starting with 0022400
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1012-2014·2014-02-26
Zimmer Recalls Asia One-Piece Lag Screws Due to Packaging Validation Issues
Zimmer is recalling 7,044,680 Asia One-Piece Lag Screws because packaging operations at a Puerto Rico facility were not properly validated, potentially affecting sterile barrier integrity.
Product
ASIA ONE-PIECE LAG SCREW
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1023-2014·2014-02-26
Zimmer Recalls Modular Hip Cup Liners Due to Packaging Validation Issues
Zimmer is recalling 7,044,680 modular hip cup liners because packaging operations at its Puerto Rico facility were not properly validated, despite passing seal integrity tests.
Product
MODULAR CUP NEUTRAL LINER MODULAR CUP 10 DEGREE LIN MODULAR CUP 20 DEGREE LIN MODULAR CUP 7MM OFFSET LI
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0983-2014·2014-02-26
Invivo Expression Information Portal Recalled for Audio Failure
Invivo Corporation is recalling the Expression Information Portal (Model IP5) because the device may fail to produce audio upon power up.
Product
Invivo Corporation Expression Information Portal (Model IP5) is intended to be used as a secondary display control unit, where the device monitors the vital signs of a patient undergoing an MRI procedure from the MR control room, induction room, or recovery room and then outputs…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1009-2014·2014-02-26
Zimmer Recalls Interlocking IM Screws and Tibial Nails Due to Packaging Validation
Zimmer is recalling interlocking IM screws and tibial nails sterile packaged at a Puerto Rico facility because packaging operations were not properly validated.
Product
INTERLOCKING IM SCREW SML, MED and LRG; M/DN TIBIAL I/M NAIL 6 MM to 15 MM. Some items starting with codes 0022530, 0022531, 002532, 0022533, 0022534
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1006-2014·2014-02-26
Zimmer Recalls Versa-FX Orthopedic Implants Due to Packaging Validation Issues
Zimmer is recalling specific Versa-FX orthopedic implant lots because packaging operations at its Puerto Rico facility were not properly validated, despite passing seal integrity tests.
Product
VERSA-FX KEYLESS 90D X 8 and X 11, VERSA-FX KEYLESS 95D X 8, X 11, and X 14, VERSA-FX KEYLESS 140D X 4 and X 5, VERSA-FX KEYLESS 135D X 4 and X 5, VERSA-FX SHORT TUBE, 130D, 135D and 140D, VERSA-FX STANDARD TUBE, 1 and VERSA-FX SPRCNDLR TUBE, 9 Item codes starting with…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1024-2014·2014-02-26
Zimmer Recalls Trilogy Acet Shell and Bone Screw Medical Devices
Zimmer is recalling Trilogy Acet Shell and Bone Screw devices due to unvalidated packaging operations at its Puerto Rico facility.
Product
TRILOGY ACET SHELL 36MM O TRILOGY ACET SHELL 38MM O TRILOGY ACET SHELL 40MM O TRILOGY ACET SHELL 42MM O TRILOGY ACET SHELL 44MM O TRILOGY ACET SHELL 46MM O TRILOGY ACET SHELL 48MM O TRILOGY ACET SHELL 50MM O TRILOGY ACET SHELL 52MM O TRILOGY ACET SHELL 54MM O TRILOGY…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1031-2014·2014-02-26
Zimmer Recalls 12/14 Femoral Heads Due to Packaging Validation Issues
Zimmer is recalling 12/14 femoral heads because packaging operations at its Puerto Rico facility were not properly validated, despite passing subsequent seal integrity tests.
Product
12/14 COCR FEMORAL HEAD (2, 3 and 4); 12/14 FEMORAL HEAD (+7X28M and 7X32M)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1021-2014·2014-02-26
Zimmer Recalls Knee Implant Components Due to Packaging Validation Issues
Zimmer is recalling specific knee implant components because packaging operations at a Puerto Rico facility were not properly validated, despite passing seal integrity tests.
Product
I/B II KNEE DOMED PATELLA, I/B II KNEE FLUTED ROD (1 and 2), MGII KNEE 10MM PATELLA (2,3 and 4), MGII KNEE SLF-TAP BONE ST
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1010-2014·2014-02-26
Zimmer Recalls Interlocking IM Screws Due to Packaging Validation Issues
Zimmer is recalling Interlocking IM Screws because packaging operations at a Puerto Rico facility were not properly validated, despite passing subsequent seal integrity tests.
Product
INTERLOCKING IM SCREW 4.5 and INTERLOCKING IM SCREW LG Some items starting with codes 0022530
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1013-2014·2014-02-26
Zimmer Recalls ITST Anti-Rotation Screws and Femoral Intramedullary Nails
Zimmer is recalling ITST anti-rotation screws and femoral intramedullary nails due to unvalidated packaging operations at its Puerto Rico facility.
Product
ITST ANTI-ROTATION SCREW and FEM IM NAIL (10MM, 11 MM, 12 MM, 13 MM, 14 MM and 15 MM) DIA X (18, 30, 32, 34, 36, 38, 40, 42, 44, 46, 48 and 50)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1036-2014·2014-02-26
Zimmer Recalls CPT Degree Taper and Femoral HD Medical Devices
Zimmer is recalling CPT Degree Taper and Femoral HD devices due to unvalidated packaging operations at a Puerto Rico facility.
Product
CPT DEGREE TAPER (various sizes) and FEMORAL HD (various sizes)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1016-2014·2014-02-26
Zimmer Recalls Hip Prostheses Due to Unvalidated Packaging Operations
Zimmer is recalling specific hip prosthesis models because packaging operations at its Puerto Rico facility were not properly validated, despite passing subsequent seal integrity tests.
Product
MOORE HIP PROS LONG FENES, MOORE HIP PROS NRW STR FE, MOORE HIP PROS STR FENEST, THOMPSON HIP PROSTHESIS 3, 4, 5 and 6.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1039-2014·2014-02-26
Zimmer Recalls Compression Screws Due to Packaging Validation Review
Zimmer is recalling 7,044,680 compression screws because packaging operations at its Puerto Rico facility were not properly validated, despite passing subsequent seal integrity tests.
Product
COMPRESSION SCREW (1/2, 1-1/2, 1-1/4, 1-3/4, 1. 2. 3/4 IN)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1040-2014·2014-02-26
Zimmer Recalls Orthopedic Screws Due to Packaging Validation Deficiencies
Zimmer is recalling 7,044,680 orthopedic screws because packaging operations at its Puerto Rico facility were not properly validated, raising concerns about sterile barrier integrity.
Product
PERI SCR. 3.5MM X 10MM PERI SCR. 3.5MM X 12MM PERI SCR. 3.5MM X 14MM PERI SCR 3.5MM X 44MM STE PERI SCR. 3.5MM X 65MM PERI. SCR 4.0MM X24MM PERI. SCR 4.0MM X40MM PERI SCR. 4.0MMX14MM FULL PERI SCR. 4.0MMX32MM FULL PERI SCR. 4.0MMX38MM FULL 3.5MM…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1020-2014·2014-02-26
Zimmer Recalls NEXGEN Osteotomy Cortical Bone Screws Due to Packaging Validation
Zimmer is recalling NEXGEN Osteotomy Cortical Bone Screws because packaging operations at a Puerto Rico facility were not properly validated, despite passing seal integrity tests.
Product
NEXGEN OSTEOTOMY CORT BON. Item codes starting with 0052500
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1027-2014·2014-02-26
Zimmer Recalls Pressfit Femoral Stems Due to Packaging Validation Issues
Zimmer, Inc. is recalling 7,044,680 units of Pressfit Femoral Stems because packaging operations at a Puerto Rico facility were not properly validated.
Product
PRESSFIT FEM ST FX 16 X 1
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1037-2014·2014-02-26
Zimmer Recalls FEM HD ION Hip Implants Due to Packaging Validation Issues
Zimmer is recalling FEM HD ION hip implants because packaging operations at a Puerto Rico facility were not properly validated, despite passing seal integrity tests.
Product
FEM HD ION (various sizes)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1028-2014·2014-02-26
Zimmer Recalls Versys Heritage Femoral Stems Due to Packaging Validation Issues
Zimmer is recalling Versys Heritage Femoral Stems because packaging operations at a Puerto Rico facility were not properly validated, raising concerns about sterile barrier integrity.
Product
VERSYS HERITAGE FEM STEM
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1002-2014·2014-02-26
Zimmer Recalls Bone Screws Due to Packaging Validation Deficiencies
Zimmer is recalling specific bone screws because packaging operations at its Puerto Rico facility were not properly validated, despite passing subsequent seal integrity tests.
Product
HERBERT MINI BONE SCREW 2 and HERBERT/WHIPPLE C ANN BONE. Items starting with 0011500 and 0011520.
Category
Medical Device
Distribution
Distributed nationwide