State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Western Drug is recalling 46 containers of Methylcobalamin Injection because there is a lack of assurance of sterility.
Halcore Group is recalling 18 model year 2015 Horton ambulances because an incorrectly installed circuit board component may cause electrical system failure, potentially disabling life-saving equipment.
Life Science Pharmacy Inc. is recalling compounded Estriol Suppositories because they may be contaminated with penicillin. The recall covers all lots distributed nationwide.
Baylis Medical Corp is recalling 433 ProTrack Microcatheters nationwide due to circumferential cracks along the shaft.
Carl Zeiss Meditec is recalling IOL Master 500 software versions 7.5 and 7.7 because calculation printouts and exported reports may contain incorrect intraocular lens power data.
Ameritrans is recalling 2012-2014 buses with Ricon wheelchair lifts where oversized pivot holes may allow bearings to shift, risking platform failure.
Life Science Pharmacy Inc. is recalling compounded Estriol Vaginal Creams due to potential penicillin cross-contamination.
Philips is recalling eight INTEGRIS cardio systems because the ceiling suspension system may fall.
Western Drug is recalling Cantharitus Multi-Mix Prep because the product lacks assurance of sterility. The recall affects all lots distributed nationwide.
Western Drug is recalling T.C.A 30% Acid Solution because the product lacks assurance of sterility. The recall affects one container distributed nationwide.
Medtronic is recalling InSync III pacemakers due to unexpected high battery impedance affecting long-term performance.
Philips Medical Systems is recalling 10 Xper vascular systems because the monitor ceiling suspension system may fall.
Carl Zeiss Meditec AG is recalling IOL Master 5.5 software versions 7.5 and 7.7 because printouts and reports may contain incorrect IOL power data.
Philips Medical Systems is recalling INTEGRIS H5000F/Allura 9F X-ray systems because the monitor ceiling suspension system may fall.
Life Science Pharmacy Inc. is recalling compounded Estriol Gels because they may be contaminated with penicillin. The recall covers all lots distributed nationwide.
Philips Medical Systems is recalling nine Allura Xper Series units because the monitor ceiling suspension system may fall.
Life Science Pharmacy Inc. is recalling Human Chorionic Gonadotropin (HCG) sublingual drops due to potential penicillin cross-contamination. The recall covers all lots distributed nationwide.
Philips Medical Systems is recalling five Allura BiPlane X-ray systems because the monitor ceiling suspension system may fall.
Quest Medical, Inc. is recalling specific MPS Delivery Sets used with cardiopulmonary bypass equipment due to intermittent seal failures during use.
Life Science Pharmacy Inc. is recalling TRI-EST Gels because they may be contaminated with penicillin.
Stryker is recalling 19,876 I.V. poles because a nonconforming latch housing may cause them to retract unexpectedly while holding medical equipment.
Western Drug is recalling Procaine HCl Injection 1% and 2% because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.
Basler Electric is recalling about 11,900 Class 2 electric transformers because a circuit breaker may fail to trip, posing fire and electrical shock risks.
Geritrex Corporation is recalling Polyethylene Glycol 3350-GRX Powder 100% jars because the FDA determined they are unapproved new drugs and misbranded.
Stryker is recalling 2,577 Duracon Tibial Wedge implants because they punctured the packaging's Tyvek lids, potentially compromising sterility.