State
73,833 recalls have nationwide distribution and so reach Northern Mariana Islands. 23 additional recalls listed Northern Mariana Islands specifically in their distribution scope.
Of the 23 recalls naming Northern Mariana Islands we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 18 (78%) are Severe.
Which agencies issued them
These figures cover only the 23 recalls whose distribution notice names Northern Mariana 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.
Pega Medical Inc. is recalling 48 units of the Fassier-Duval IM Telescopic System because the outer package label listed the incorrect device length.
Altasource LLC dba Meta Labs LLC is recalling Nice-En-Smooth Berry Burst lubricant because the firm is not registered as a drug manufacturer.
GlaxoSmithKline is recalling Nicorette 2 mg lozenges because they failed specifications for thickness, softness, and potency.
Pfizer is recalling Tikosyn (dofetilide) 500 mcg capsules because a single 250 mcg capsule was found in one bottle. The recall covers 23,064 bottles distributed nationwide.
P&L Developments, LLC is recalling 2,500,510 bottles of Day Time Cold & Flu because the phenylephrine component is subpotent.
Merit Medical Systems is voluntarily recalling specific lots of Laureate Hydrophilic Guide Wires due to a discrepancy between carton and unit labeling.
GlaxoSmithKline is recalling Nicorette 4 mg lozenges because they failed specifications for thickness, softness, and potency.
Zimmer, Inc. is recalling 17 units of Trabecular Metal Modular Acetabular System shells because the locking ring was missing.
Merit Medical Systems is recalling 173 units of Laureate Hydrophilic Guide Wire due to a labeling discrepancy where the product was mixed with a different lot.
Altasource LLC is recalling Mega-Gen His and Hers Personal Lubricant because the firm is not registered as a drug manufacturer.
BioMerieux SA is recalling ZYM B Reagent (REF 70493) because a visual defect and activity issue can cause false negative results in microbiological tests.
Siemens is recalling 490 ACUSON X700 ultrasound systems because previous patient data may replace current patient dates in reports.
Abbott Molecular is recalling 20 kits of CEP 8 SG ASR Probe that contained the wrong probe. The kits contained Vysis CEP 4 probe instead of the expected CEP 8 probe.
GlaxoSmithKline is recalling specific lots of Nicorette 4 mg lozenges because they failed quality specifications, including being overly thick, soft, and sub or superpotent.
GlaxoSmithKline is recalling specific lots of Nicorette 2 mg lozenges because they failed quality specifications, including being overly thick, soft, and sub or superpotent.
GlaxoSmithKline is recalling specific lots of Nicorette lozenges because they failed quality specifications, including being overly thick, soft, and sub or superpotent.
Altasource LLC dba Meta Labs LLC is recalling 155 units of Hot Ice topical gel because the firm is not registered as a drug manufacturer.
Altasource LLC is recalling 70 units of Amo-O Herbal Stimulator gel because the firm is not registered as a drug manufacturer.
BioMerieux is recalling ZYM B and FB reagents because a visual defect and activity issue can cause false negative results in Rapid ID 32 strips and API biochemical tests.
GlaxoSmithKline is recalling Nicorette and store-brand nicotine lozenges because they failed quality specifications, including being overly thick, soft, and sub or superpotent.
Branan Medical is recalling ToxCup Drug Screen Cups because the lid labels may contain incorrect result interpretation graphics.
Boston Scientific is recalling 9 iLab Ultrasound Imaging Systems because a software update may cause the Longview distance measurement to display double the actual value.
GlaxoSmithKline is recalling Nicorette and store-brand nicotine lozenges because they failed specifications for thickness, softness, and potency.
Arrow International Inc. is recalling 789 units of Arrow Pressure Injectable PICC catheters because they contain a 40cm catheter instead of the required 50cm catheter.
Upsher Smith Laboratories is recalling 36 bottles of Oxandrolone Tablets, USP, 10 mg, because they were packaged without primary labels.