State

US Virgin Islands product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

57476–57500 of 74005

ModerateFDA (Drugs)·D-1548-2014·2014-08-27
US Compounding Recalls Mislabeled Ephedrine Sulfate Injection Syringes
US Compounding Inc is recalling 762 syringes of ephedrine sulfate injection due to a labeling error on the outer protective bags that could cause confusion regarding the drug's strength.
Product
ePHEDrine Sulfate Injection, USP 25 mg/5 mL (5 mg/mL) Single Use 5 mL Syringe, For IV, IM, or SC injection, Preservative Free, For Office/Hospital Use Only, Protect from Light, 62295-3084-05, US Compounding Pharmacy, Conway, AR 800-718-3588
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2273-2014·2014-08-27
AMO Tecnis CL Intraocular Lenses Recalled for Incorrect Diopter Labeling
AMO Puerto Rico Manufacturing is recalling 77,055 Tecnis CL intraocular lenses because units may be labeled with the incorrect diopter power.
Product
AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002. Indicated for primary implantation for the visual correction of aphakia in adult patients. Tecnis CL Mono 13 mm with the following diopter sizes: 11.0 and 11.5 Product Usage: AMO TECNIS CL monofocal…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2248-2014·2014-08-27
Zimmer Recalls 6.5 mm Cancellous Screws Due to Leak Test Failures
Zimmer, Inc. is recalling 47,682 units of 6.5 mm Cancellous Screws because they failed a leak test due to damage of the inner cavity.
Product
6.5 mm Cancellous Screw 32 mm Thread Length Sterile zimmer
Category
Medical Device
Distribution
45 states
ModerateFDA (Devices)·Z-2244-2014·2014-08-27
Zimmer Recalls Magna-Fx Cannulated Bone Screws Due to Leak Test Failures
Zimmer, Inc. is recalling 47,682 units of Magna-Fx Cannulated Bone Screws because they failed leak tests due to inner cavity damage.
Product
Magna-Fx Cannulated Screw Fixation System Bone Screw Fully Threaded Sterile zimmer
Category
Medical Device
Distribution
45 states
ModerateFDA (Devices)·Z-2275-2014·2014-08-27
AMO TECNIS CL Intraocular Lenses Recalled for Incorrect Diopter Labeling
AMO Puerto Rico Manufacturing is recalling 77,055 TECNIS CL intraocular lenses because they may be labeled with the incorrect diopter power.
Product
AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002. Indicated for primary implantation for the visual correction of aphakia in adult patients. Tecnis CL Mono 13 mm with the following diopter sizes: 13.0, 13.5, 14.0 Product Usage: AMO TECNIS CL monofocal…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2272-2014·2014-08-27
AMO Tecnis CL Intraocular Lenses Recalled for Incorrect Diopter Labeling
AMO Puerto Rico Manufacturing is recalling 77,055 Tecnis CL intraocular lenses because units may be labeled with the incorrect diopter power.
Product
AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002. Indicated for primary implantation for the visual correction of aphakia in adult patients. Tecnis CL Mono 13 mm with the following diopter sizes: 10.0 and 10.5 Product Usage: AMO TECNIS CL monofocal…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2281-2014·2014-08-27
AMO Tecnis CL Intraocular Lenses Recalled for Incorrect Diopter Power Labeling
AMO Puerto Rico Manufacturing is recalling 77,055 Tecnis CL intraocular lenses because they may be labeled with the incorrect diopter power.
Product
AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002. Indicated for primary implantation for the visual correction of aphakia in adult patients. Tecnis CL Mono 13 mm with the following diopter sizes: 19.5-20 Product Usage: AMO TECNIS CL monofocal foldable…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2277-2014·2014-08-27
AMO TECNIS CL Intraocular Lenses Recalled for Incorrect Diopter Power Labeling
AMO Puerto Rico Manufacturing is recalling 77,055 TECNIS CL intraocular lenses because units may be labeled with the incorrect diopter power.
Product
AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002. Indicated for primary implantation for the visual correction of aphakia in adult patients. Tecnis CL Mono 13 mm with the following diopter sizes: 15.5, 16.0 Product Usage: AMO TECNIS CL monofocal foldable…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2251-2014·2014-08-27
Zimmer Recalls 4.0 mm Cancellous Screws Due to Leak Test Failures
Zimmer, Inc. is recalling 47,682 units of 4.0 mm Cancellous Screws because they failed leak tests due to inner cavity damage.
Product
4.0 mm Cancellous Screw, Partially Threaded Sterile Zimmer
Category
Medical Device
Distribution
45 states
ModerateFDA (Drugs)·D-1541-2014·2014-08-27
Wockhardt Recalls Metoprolol Succinate Tablets for Dissolution Failures
Wockhardt USA is recalling specific lots of Metoprolol Succinate Extended-Release Tablets because they failed dissolution testing. The recall covers 11,661 bottles distributed nationwide.
Product
Wockhardt Metoprolol Succinate Extended-Release Tablets, USP 200 mg, a) 100-count bottle (NDC 64679-737-02), b) 500-count bottle (NDC 64679-737-03) Rx only, Manufactured by: Wockhardt Limited Mumbai, India Distributed by: Wockhardt USA LLC 20 Waterview Boulevard. Parsippany, NJ…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2247-2014·2014-08-27
Zimmer Recalls 6.5 mm Cancellous Trauma Screws Due to Leak Test Failures
Zimmer, Inc. is recalling 47,682 units of 6.5 mm Cancellous Trauma Screws because they failed leak tests due to inner cavity damage.
Product
6.5 mm Cancellous Screw 16 mm Thread Length Sterile zimmer
Category
Medical Device
Distribution
45 states
ModerateFDA (Devices)·Z-2284-2014·2014-08-27
AMO TECNIS CL Intraocular Lenses Recalled for Incorrect Diopter Labeling
AMO Puerto Rico Manufacturing is recalling specific Tecnis CL intraocular lenses because they may be labeled with the incorrect diopter power.
Product
AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002. Indicated for primary implantation for the visual correction of aphakia in adult patients. Tecnis CL Mono 13 mm with the following diopter sizes: 23, 23.5 & 24. Product Usage: AMO TECNIS CL monofocal…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1544-2014·2014-08-27
Triveen PRx RNF Capsules Recalled for Incorrect Vitamin B12 Labeling
Trigen Laboratories is recalling Triveen PRx RNF Capsules because the label lists Vitamin B12, which is not in the formulation.
Product
Triveen - PRx RNF Capsules, 30-count bottles, Rx only; Manufactured for: Trigen Laboratories, Inc., Sayreville, NJ 08872, NDC 13811-558-30, UPC 3 13811 55830 2.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1539-2014·2014-08-27
Mylan Recalls Tolterodine Tartrate Tablets Due to Impurity Failures
Mylan Pharmaceuticals is recalling 9,225 bottles of Tolterodine Tartrate Tablets, 1 mg, because the product failed impurity specifications for lactol and total impurities.
Product
Tolterodine Tartrate Tablets, 1 mg, 60 Tablet Bottles, Rx only. Mylan Pharmaceuticals Inc., Morgantown, WV 26505. NDC: 0378-5445-91.
Category
Drug
Distribution
Distributed nationwide
SevereCPSC·14262·2014-08-26
Hewlett-Packard Recalls Notebook Computer AC Power Cords Due to Fire and Burn Hazards
Hewlett-Packard is recalling specific AC power cords for notebook computers because they can overheat, posing a fire and burn hazard.
Product
Hewlett-Packard and Compaq notebook computer AC power cords
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·14E056000·2014-08-26
Agility Fuel Systems Recalls CNG Fuel Hoses Due to Corrosion Risk
Agility Fuel Systems is recalling specific CNG fuel systems because a hose component may corrode and leak gas, increasing fire risk.
Product
FUEL SYSTEM, OTHER:DELIVERY:HOSES, LINES/PIPING, AND FITTINGS recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V517000·2014-08-26
NABI Transit Bus Recall for CNG Fuel Tank Abrasion Risk
NABI is recalling 2012-2014 31LFW and 40LFW transit buses because CNG fuel tanks may be abraded by pressure relief devices, increasing fire risk.
Product
NABI — NABI 40LFW, 31LFW
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V516000·2014-08-26
Audi Recalls 2013 Q7 Vehicles Due to Brake Booster Oil Leak Risk
Volkswagen is recalling 2013 Audi Q7 vehicles with 3.0L TDI engines because engine oil may leak into the brake booster, potentially causing a loss of power braking assist.
Product
AUDI — AUDI Q7
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·14V515000·2014-08-26
Jayco Recalls 2015 Seismic Fifth Wheels for Incorrect Cargo Labels
Jayco is recalling 2015 Seismic fifth wheel trailers because incorrect cargo capacity labels may lead to overloading, tire failure, and crashes.
Product
JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL SEISMIC
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·14E057000·2014-08-26
Navistar Recalls Warning Triangle Kits for Inadequate Light Reflection
Navistar is recalling FLTTRIKIT3 warning triangle kits manufactured between August 2012 and July 2014 because they may not reflect enough light to warn other drivers.
Product
EQUIPMENT recall
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·14746·2014-08-26
Cree Recalls LED High-Bay Luminaires Due to Laceration Hazard
Cree is recalling approximately 10,000 LED high-bay luminaires because the tempered glass lens can break, posing a laceration hazard. No injuries have been reported.
Product
LED High-Bay Luminaires
Category
Consumer Product
Distribution
Distributed nationwide
CriticalCPSC·14261·2014-08-22
Ace Bayou Bean Bag Chairs Recalled Due to Suffocation and Choking Hazards
Ace Bayou is recalling about 2.2 million bean bag chairs because zippers can open, allowing children to crawl inside and suffocate or choke on foam beads.
Product
Bean bag chairs
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·14V514000·2014-08-22
Ford Recalls 2014 Focus and C-Max for Steering Gear Assembly Defect
Ford is recalling 2014 Focus and C-Max vehicles manufactured in August 2014 due to incorrectly assembled steering gears that may cause loss of steering control.
Product
FORD — FORD FOCUS, C-MAX
Category
Vehicle
Distribution
Distributed nationwide
CriticalUSDA FSIS·054-2014·2014-08-21
APPA Fine Foods Recalls Chicken Caesar Salad Kits for Listeria
APPA Fine Foods is recalling approximately 92,657 pounds of chicken Caesar salad kits due to possible Listeria monocytogenes contamination.
Product
California Firm Recalls Chicken Caesar Salad Kits For Possible Listeria Contamination
Category
Food
Distribution
Distributed nationwide
HighCPSC·14745·2014-08-21
StoveTop FireStop Microhood Recalled Due to Fire Suppression Failure Risk
WilliamsRDM is recalling StoveTop FireStop Microhood units because the front canister may fall off and fail to suppress fires. No injuries have been reported.
Product
The StoveTop FireStop® Microhood™ Fire Suppressors
Category
Consumer Product
Distribution
Distributed nationwide