State
73,806 recalls have nationwide distribution and so reach US Virgin Islands. 178 additional recalls listed US Virgin Islands specifically in their distribution scope.
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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
The Anspach Effort, Inc. is recalling 10.5cm Long Attachments for pneumatic systems because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 41 units of the 19cm Attachment, Black Max, because the supplied directions for use did not include a recommended service interval.
The Anspach Effort, Inc. is recalling 198 units of the 7.2cm Adjustable Drill Guide because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 22 Minimal Access Attachments because the supplied directions for use did not contain a recommended service interval.
Breg Inc is recalling approximately 2,609 sterile dressings because a small percentage may have unsealed pouches, rendering them non-sterile.
The Anspach Effort, Inc. is recalling 206 units of the 20.2cm Heavy Duty Long Heavy Short Attachment because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling six units of the Adjustable Drill Guide, Black Max because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 148 Standard Craniotomes because the supplied directions for use did not include a recommended service interval.
The Anspach Effort, Inc. is recalling 17 units of the 16.5cm Micro Revision Attach because the supplied directions for use did not include a recommended service interval.
The Anspach Effort, Inc. is recalling 14 IMRI Short Attachment units because the supplied directions for use did not include a recommended service interval.
Breg Inc is recalling 2,609 units of If Hip Sterile Polar Dressings because some may have unsealed pouches, rendering them non-sterile.
The Anspach Effort, Inc. is recalling three Pediatric Craniotomes because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 98 Minimal Access Straight Drivers because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 203 units of the 10.5cm QD Angle Attachment because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 2,339 units of the 5.0cm Heavy Duty Short Attachment because the supplied directions for use did not contain a recommended service interval.
Tradewind Foods is recalling Goya Octopus in Olive Oil because the product contains squid instead of octopus. This labeling error affects consumers in Puerto Rico and the Caribbean.
The Anspach Effort, Inc. is recalling 207 Electronic Foot Controls because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 9,829 pneumatic attachments because the supplied directions for use did not include a recommended service interval.
Smith & Nephew is recalling Renovation Thin Osteotome Blades because stability data does not support the labeled 10-year shelf life.
The Anspach Effort, Inc. is recalling 293 eMax2 Hybrid Hand Controls because the supplied directions for use did not contain a recommended service interval.
Fagron, Inc. is recalling Zinc Oxide Paste 25% because of an incorrect strength value in the Drug Facts Panel.
The Anspach Effort, Inc. is recalling 25 BLACKMAX-NEURO LOW PRESSURE pneumatic systems because the supplied directions for use did not include a recommended service interval.
The Anspach Effort, Inc. is recalling 7.5cm Angle Attachments because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 13.5CM Angle Attachments because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 16 Small Attachment, J-Latch units because the supplied directions for use did not contain a recommended service interval.