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.

59801–59825 of 74011

HighFDA (Devices)·Z-0779-2014·2014-01-22
Anspach MIA 16 Minimally Invasive Attachment Recalled for Sterility Failure
The Anspach Effort, Inc. is recalling 183 Anspach MIA 16 attachments because they did not reach the expected sterility assurance level.
Product
Anspach MIA 16 (16cm Minimally Invasive Attachment), Rx Only MIA16 attachments are intended for use with Motor Systems for cutting and shaping bones, including the spine and cranium.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0721-2014·2014-01-22
Boston Scientific Recalls TWISTER PLUS Retrieval Devices Due to Seal Integrity
Boston Scientific is recalling TWISTER PLUS 22mm Rotatable Retrieval Devices because the pouch seal integrity may be compromised, potentially affecting sterility.
Product
TWISTER PLUS 22mm Rotatable Retrieval Device (Box of 10 configuration) Universal Product Number (UPN):M00561412. Distributed by: Boston Scientific, Natick, MA. Manufactured by: Horizons International Corp., Costa Rica Intended to be used in flexible endoscopes as a retrieval…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·14083·2014-01-22
Midwest-CBK Recalls Baby Rattles Due to Choking Hazard
Midwest-CBK is recalling about 1,900 baby rattles because the head can detach, posing a choking hazard to young children.
Product
Baby rattles
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0719-2014·2014-01-22
Boston Scientific Recalls TWISTER PLUS Retrieval Devices Due to Seal Integrity Issues
Boston Scientific is recalling TWISTER PLUS 22mm Rotatable Retrieval Devices because the pouch seal integrity may be compromised, potentially affecting sterility.
Product
TWISTER PLUS 22mm Rotatable Retrieval Device (Box of 1 configuration) Universal Product Number (UPN): M00561410. Distributed by: Boston Scientific. Manufactured by: Horizons International Corp. Intended to be used in flexible endoscopes as a retrieval device for foreign…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0728-2014·2014-01-22
Anspach Carbide Cutting Burrs Recalled Due to Fracture During Use
The Anspach Effort, Inc. is recalling carbide cutting burrs and drums because some fractured during use. The products are used for cutting and shaping bone.
Product
Anspach Carbide Cutting Burrs & Drums: 1.5MM x 7.5MM Cylindrical Carbide Drum part # S-15DRMC Anspach cutting burrs are intended for cutting and shaping bone, including the spine and cranium
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0770-2014·2014-01-22
Teleflex Recalls Electrosurgical Suction Tubes Due to Sterility Concerns
Teleflex Medical is recalling 17,450 electrosurgical coagulation suction tubes because sterility cannot be guaranteed. The devices were distributed nationwide.
Product
Weck, Electrosurgical Coagulation Suction Tube 6 (15.2cm), 11 French, with Stylet, Teleflex Medical, Research Triangle, NC 2770. Intended to remove tissue and control bleeding by use of high-frequency electrical current.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0727-2014·2014-01-22
Anspach Carbide Cutting Burrs Recalled Due to Fracture During Use
The Anspach Effort, Inc. is recalling specific carbide cutting burrs because some fractured during use. The devices are intended for cutting and shaping bone.
Product
Anspach Carbide Cutting Burrs: 1.5MMx7.5MM Cylindrical Carbide Drum part # S-15DRMC-L, 1MM Carbide Fluted ball, Extended part # S-1B-C, 1MM Carbide Fluted ball part # S-SB-C, 2MM Carbide Fluted ball part # S-2SB-C, 3MM Carbide Fluted ball Extended part # S-3B-C, 3MM Carbide…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0718-2014·2014-01-22
Anspach Bone Cutting Burs Recalled for Potential Sterile Barrier Breach
The Anspach Effort, Inc. is recalling single-use sterile bone cutting burs and irrigation clips due to observed layer separation that may compromise the sterile barrier.
Product
Anspach Single Use Sterile Bone Cutting Burs and Irrigation Clips. Rx Only
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0738-2014·2014-01-22
Atrium Ocean Water Seal Chest Drain ATS Blood Recovery System Recalled
Atrium Medical Corporation is recalling 361 units of the Ocean Water Seal Chest Drain ATS Blood Recovery System because the tubing may leak or disconnect.
Product
Atrium Ocean Water Seal Chest Drain ATS (Autotransfusion) Blood Recovery System Dual patient lines with stopcock and in-line connectors Product Code: 2052-000. To evacuate air and/or fluid from the chest cavity or mediastinum.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·14085·2014-01-22
Nationwide Trident Pool Gate Latches Recalled for Magnet Failure
Nationwide Industries is recalling Trident Pool Gate Latches because the magnet can come loose, preventing the gate from securing. No injuries were reported.
Product
Nationwide Industries Trident Pool Gate Latches
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0768-2014·2014-01-22
Anspach Micro Curved Attachment Cutting Burrs Recalled for Labeling Issues
The Anspach Effort, Inc. is recalling all lots of MCA Cutting Burrs and Dissection Tools because the indications for use were broader than validated and directions were unclear.
Product
MCA7-2SB - 2MM Fluted Ball, 7.3CM. All lots are included in recall. Intended for use in cutting and shaping delicate bone material, primarily in otologic procedures such as cochleostomy.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0734-2014·2014-01-22
Remel Recalls Oxoid Antimicrobial Susceptibility Testing Discs Due to Impregnation Defect
Remel Inc is recalling Oxoid Antimicrobial Susceptibility Testing Discs because individual discs may not be sufficiently impregnated with antibiotic, resulting in smaller than expected zone sizes.
Product
Oxoid Antimicrobial Susceptibility Testing Disc, MEM10, REF: CT0774B, 10 mcg meropenem, Packed in packs containing 5 cartridges per pack, 50 discs per cartridge. Firm name on the label is Oxoid, Ltd., Basingstoke, United Kingdom. Used in the semi-quantitative agar diffusion…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0715-2014·2014-01-22
Anspach MCA Cutting Burr Recalled for Inadequate Labeling Instructions
The Anspach Effort, Inc. is recalling MCA Cutting Burs because the current directions for use do not provide sufficient details regarding the intended use for these specific burs.
Product
Anspach MCA Cutting Burr, DFU Rx Only Designed for cutting and shaping delicate bone, primarily in otology procedures
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0731-2014·2014-01-22
GE Centricity PACS System Recalled for Potential Image Loss During Transfer
GE Healthcare is recalling Centricity PACS System versions 3.X and 4.X due to a potential loss of diagnostic images during transfers between servers.
Product
Centricity PACS System versions 3.X and higher and 4.X and higher Product Usage: The Centricity PACS Workstation is intended for use as a primary diagnostic and analysis tool for diagnostic images by trained healthcare professionals, including radiologists, physicians…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0725-2014·2014-01-22
GE Healthcare Recalls Mobile X-ray Systems Due to Software Display Issue
GE Healthcare is recalling 1,027 Optima XR220amx and XR200amx mobile X-ray systems due to a software issue that may cause patient exams to display incorrectly.
Product
GE Optima XR220amx and Optima XR200amx with Digital Upgrade Mobile Radiographic Systems. Model numbers 5555000-5, 5555000-6, and 5421698.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0756-2014·2014-01-22
Anspach Micro Curved Attachment Cutting Burrs Recalled for Labeling Errors
The Anspach Effort, Inc. is recalling MCA Cutting Burrs and Dissection Tools because the indications for use were broader than the device's validation.
Product
MCA5-1SB - 1MM Fluted Ball, 5.6CM. All lots are included in recall. Intended for use in cutting and shaping delicate bone material, primarily in otologic procedures such as cochleostomy.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0753-2014·2014-01-22
Anspach Micro Curved Attachment Cutting Burrs Recalled for Labeling Errors
The Anspach Effort, Inc. is recalling MCA Cutting Burrs and Dissection Tools because the indications for use were broader than validated and directions were unclear.
Product
MCA5-08SD - 0.8MM Diamond Ball, 5.6CM. All lots are included in recall. Intended for use in cutting and shaping delicate bone material, primarily in otologic procedures such as cochleostomy.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0758-2014·2014-01-22
Anspach Micro Curved Attachment Cutting Burrs Recalled for Labeling Errors
The Anspach Effort, Inc. is recalling all lots of MCA Cutting Burrs and Dissection Tools because the indications for use were broader than the device's validation.
Product
MCA5-2SB - 2MM Fluted Ball, 5.6CM. All lots are included in recall. Intended for use in cutting and shaping delicate bone material, primarily in otologic procedures such as cochleostomy.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0762-2014·2014-01-22
Anspach Micro Curved Attachment Cutting Burrs Recalled for Labeling Errors
The Anspach Effort, Inc. is recalling all lots of MCA Cutting Burrs and Dissection Tools because the indications for use were broader than validated and directions for use were unclear.
Product
MCA7-07SD - 0.7MM Diamond Ball, 7.3CM. All lots are included in recall. Intended for use in cutting and shaping delicate bone material, primarily in otologic procedures such as cochleostomy.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-407-2014·2014-01-22
B. Braun Recalls Sodium Chloride Injection Due to Incorrect Bar Code Labeling
B. Braun Medical Inc. is recalling 19,572 bags of 0.45% Sodium Chloride Injection because the bar code incorrectly identifies the product as Potassium Chloride.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0765-2014·2014-01-22
Anspach Micro Curved Attachment Cutting Burrs Recalled for Labeling Errors
The Anspach Effort, Inc. is recalling all lots of MCA Cutting Burrs and Dissection Tools because the indications for use were broader than the device's validation and directions for use were unclear.
Product
MCA7-15SD - 1.5MM Diamond Ball, 7.3CM. All lots are included in recall. Intended for use in cutting and shaping delicate bone material, primarily in otologic procedures such as cochleostomy.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0766-2014·2014-01-22
Anspach Micro Curved Attachment Cutting Burrs Recalled for Labeling Errors
The Anspach Effort, Inc. is recalling all lots of MCA Cutting Burrs and Dissection Tools because the indications for use were broader than the device's validation.
Product
MCA7-1SB - 1MM Fluted Ball, 7.3CM. All lots are included in recall. Intended for use in cutting and shaping delicate bone material, primarily in otologic procedures such as cochleostomy.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0767-2014·2014-01-22
Anspach Micro Curved Attachment Cutting Burrs Recalled for Labeling Errors
The Anspach Effort, Inc. is recalling MCA Cutting Burrs and Dissection Tools because the indications for use were broader than validated and directions were unclear.
Product
MCA7-1SD - 1MM Diamond Ball, 7.3CM. All lots are included in recall. Intended for use in cutting and shaping delicate bone material, primarily in otologic procedures such as cochleostomy.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0769-2014·2014-01-22
Anspach Micro Curved Attachment Cutting Burrs Recalled for Labeling Errors
The Anspach Effort, Inc. is recalling all lots of MCA Cutting Burrs and Dissection Tools because the indications for use were broader than the device's validation.
Product
MCA7-2SD - 2MM Diamond Ball, 7.3CM. All lots are included in recall. Intended for use in cutting and shaping delicate bone material, primarily in otologic procedures such as cochleostomy.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0712-2014·2014-01-22
Boston Scientific Extractor Pro XL Retrieval Balloon Catheter Recall
Boston Scientific is recalling 34 units of Extractor Pro XL Retrieval Balloon Catheters due to potential incorrect skive hole location or balloon size.
Product
Boston Scientific Extractor Pro XL Retrieval Balloon Catheter 12-15 mm Injects Below UPN :M00547140
Category
Medical Device
Distribution
Distributed nationwide