State

Northern Mariana Islands product recalls

73,833 recalls have nationwide distribution and so reach Northern Mariana Islands. 23 additional recalls listed Northern Mariana Islands specifically in their distribution scope.

What the numbers show

Total: 23
Critical: 0
Severe: 18
Most recent: 2026-09-23

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.

58876–58900 of 73856

ModerateFDA (Devices)·Z-1256-2014·2014-03-26
Zimmer Recalls Natural-Knee II Constrained Knee System Tibia Components
Zimmer, Inc. is recalling 3,638 units of Natural-Knee II Constrained Knee System tibia components due to discoloration caused by premature oxidation.
Product
Natural-Knee¿ II Constrained Knee System NKII CCK TIB INS SZ00/0-L NKII CCK TIB INS SZ1/2-LF NKII CCK TIB INS SZ3-5 -L NKII CCK TIB INS SZ00/0-R NKII CCK TIB INS SZ3-5 -R NKII CCK TIB INS SZ1/2-LF NKII CCK TIB INS SZ3-5 -L NKII CCK TIB INS SZ00/0-R NKII CCK TIB INS…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1165-2014·2014-03-26
Traxx Recalls Guaifenesin API Powder Due to Foreign Matter
Traxx International Corp is recalling Guaifenesin API powder because it may contain polyethylene fibers from a sifting screen.
Product
Guaifenesin USP, 50 Kg Drums, CAS No. 93-14-1, Reg. No. 05436, Caution: For Manufacturing, Processing, or Repacking, Delta Synthetic Co., Ltd. 15, Minsheng St., Tucheng Dist., New Taipei City, 23679, Taiwan (ROC), NDC 60203-1001
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1242-2014·2014-03-26
Biomet Recalls Intramedullary Bone Saw CAM Assembly Due to Labeling Error
Biomet, Inc. is recalling specific lots of the Intramedullary Bone Saw CAM Assembly because the Saw Blade Assembly was incorrectly identified as a CAM Assembly.
Product
Part 475620 Intramedullary Bone Saw CAM Assembly Size 12mm, A unique and exclusive clinical instrument used to correct leg length, or rotational discrepancies in the femur.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1253-2014·2014-03-26
Zimmer Recalls Natural-Knee/Apollo Knee Implants Due to Discoloration
Zimmer, Inc. is recalling 3,638 Natural-Knee/Apollo knee implants because a component was discolored due to premature oxidation.
Product
Natural-Knee¿/Apollo" Knee: M/B PAT SZ0 NATURAL-KNEE M/B PAT SZ1 NATURAL-KNEE M/B PAT SZ2 NATURAL-KNEE
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1168-2014·2014-03-26
Perrigo Recalls Clindamycin Oral Solution Due to Particulate Matter
Paddock Laboratories is recalling seven lots of Perrigo Clindamycin Palmitate Hydrochloride for Oral Solution due to the presence of particulate matter.
Product
Perrigo, Clindamycin Palmitate Hydrochloride for Oral Solution, USP, 75mg/5mL, 100 ml, NDC 0574-0129-01
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1252-2014·2014-03-26
Zimmer Recalls Natural-Knee II Unicompartmental Knee System Components
Zimmer, Inc. is recalling specific Natural-Knee II unicompartmental knee system tibia components due to discoloration caused by premature oxidation during storage.
Product
Natural-Knee¿ II Unicompartmental Knee System: UNI ALL-POLY TIB SZ 1-7mm UNI ALL-POLY TIB SZ 1-9mm
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1244-2014·2014-03-26
Biomet Recalls Intramedullary Bone Saw Cam Assemblies Due to Labeling Error
Biomet, Inc. is recalling specific lots of Intramedullary Bone Saw Cam Assemblies because they were incorrectly labeled as Saw Blade Assemblies.
Product
Part 475630, Intramedullary Bone Saw, Cam Assembly Size 14 mm, The Biomet Intramedullary Bone Saw is a unique and exclusive clinical instrument that is used to correct leg length, or rotational discrepancies in the femur.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1255-2014·2014-03-26
Zimmer Recalls Natural-Knee II System Components Due to Discoloration
Zimmer, Inc. is recalling 3,638 units of Natural-Knee II System components due to discoloration caused by premature oxidation. The affected devices were stored in transparent containers exposed to light.
Product
Natural-Knee¿ II System ULTRA CONG INS LT SZA/9MM ULTRA CONG INS LT SZA/13M ULTRA CONG INS LT SZA/19M ULTRA CONG INS RT SZA/9MM ULTRA CONG INS RT SZA/11M ULTRA CONG INS RT SZA/13M ULTRA CONG INS RT SZA/19M ULTRA CONG INS LT SZB/13M ULTRA CONG INS LT SZB/16M ULTRA CONG…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1251-2014·2014-03-26
Zimmer Recalls Natural-Knee II Prosthesis Due to Discoloration
Zimmer, Inc. is recalling 3,638 units of Natural-Knee II knee prostheses because a component was found to be discolored due to premature oxidation.
Product
Natural-Knee¿ II - Unicompartmental Knee Prosthesis: CONG TIB INS SZ1/2 9MM UN CONG TIB INS SZ1/2 11MM U CONG TIB INS SZ1/2 13MM U CONG TIB INS SZ3/4 9MM UN CONG TIB INS SZ3/4 11MM U CONG TIB INS SZ3/4 13MM U CONG TIB INS SZ 5/6 9MM U CONG TIB INS SZ5/6 11MM U CONG TIB…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1210-2014·2014-03-26
DeRoyal Cotton Adjustable Limb Holders Recalled for Moldy Smell
DeRoyal Industries is recalling 8,962 pairs of cotton adjustable limb holders due to a moldy smell. The products were distributed in the US and Argentina.
Product
DeRoyal(R) LIMB HOLDERS, COTTON ADJUSTABLE, UNIVERSAL, REF M2017 Product Usage: Limb holders are intended for mildly to moderate agitated or disoriented patients who disrupt medical treatment and/or cause harm to themselves and/or others
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1257-2014·2014-03-26
Zimmer Recalls Natural-Knee II Tibial Inserts Due to Discoloration
Zimmer, Inc. is recalling 3,638 Natural-Knee II Posterior Stabilized Condylar Tibial Inserts because free radical oxidation caused discoloration.
Product
Natural-Knee¿ II Posterior Stabilized (P.S.) Condylar Tibial Inserts: N-K II CONS PS TIB INS SZ N-K II CONS PS TIB INS SZ N-K II CONS PS TIB INS SZ N-K II CONS PS TIB INS SZ N-K II CONS PS TIB INS SZ N-K II CONS PS TIB INS SZ N-K II CONS PS TIB INS SZ N-K II CONS PS INS…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1260-2014·2014-03-26
Zimmer Recalls Apollo Knee System Tibia Inserts Due to Discoloration
Zimmer, Inc. is recalling 3,638 Apollo Knee System tibia inserts because free radical oxidation caused discoloration. The issue resulted from improper storage conditions prior to packaging.
Product
Apollo" Knee System: PS TIB INS SZ0/16MM APOLL PS TIB INS SZ0/19MM APOLL PS TIB INS SZ0/22MM APOLL PS TIB INS SZ1/16MM APOLL PS TIB INS SZ2/16M APOLLO PS TIB INS SZ2/22MM APOLL PS TIB INS SZ3/16MM APOLL PS TIB INS SZ3/19MM APOLL PS TIB INS SZ4/9MM APOLLO PS TIB INS…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1261-2014·2014-03-26
Zimmer Recalls Apollo Revision Knee System Tibia Inserts Due to Discoloration
Zimmer, Inc. is recalling 3,638 Apollo Revision/Constrained Knee System tibia inserts because they were discolored due to premature oxidation during storage.
Product
Apollo" Revision/Constrained Knee System: SZ0-16MM AK CCK TIB INSER SZ1-11MM AK CCK TIB INSER SZ1-16MM AK CCK TIB INSER SZ1-22MM AK CCK TIB INSER SZ1-30MM AK CCK TIB INSER SZ2-11MM AK CCK TIB INSER SZ2-13MM AK CCK TIB INSER SZ2-16MM AK CCK TIB INSER SZ2-22MM AK CCK TIB…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1243-2014·2014-03-26
Biomet Recalls Intramedullary Bone Saw Cam Assemblies Due to Labeling Error
Biomet is recalling 10 Intramedullary Bone Saw Cam Assemblies because they were incorrectly labeled as Saw Blade Assemblies.
Product
Part 475625, Intramedullary Bone Saw, Cam Assembly Size 13 mm, The Biomet Intramedullary Bone Saw is a unique and exclusive clinical instrument that is used to correct leg length, or rotational discrepancies in the femur.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1259-2014·2014-03-26
Zimmer Recalls Apollo Knee Tibial Baseplates Due to Discoloration
Zimmer, Inc. is recalling 3,638 Apollo Knee Tibial Baseplates and Inserts because free radical oxidation caused discoloration in some units.
Product
Apollo Knee Tibial Baseplate/Knee Tibial Insert: CONG TIB INS SZ0/19MM APO CONG TIB INS SZ0/22MM APO CONG TIB INS SZ1/9MM APOL CONG TIB INS SZ1/11MM APO CONG TIB INS SZ1/19MM APO CONG TIB INS SZ2/13MM APO CONG TIB INS SZ2/19MM APO CONG TIB INS SZ3/9MM APOL CONG TIB INS…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1258-2014·2014-03-26
Zimmer Recalls Apollo Knee System Patella Components Due to Discoloration
Zimmer, Inc. is recalling 3,638 units of Apollo Knee System patella components due to discoloration caused by premature oxidation during storage.
Product
Apollo" Knee System: APOLLO PATELLA SZ0 28MM R
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1172-2014·2014-03-26
Noven Recalls Daytrana Patches Due to Defective Delivery System
Noven Pharmaceuticals is recalling Daytrana (methylphenidate) transdermal patches because out-of-specification results indicate the release liner may be difficult to remove.
Product
DAYTRANA — DAYTRANA (METHYLPHENIDATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1248-2014·2014-03-26
Zimmer Recalls Natural-Knee Flex System Components Due to Discoloration
Zimmer, Inc. is recalling 3,638 units of the Natural-Knee Flex System due to discoloration caused by premature oxidation during storage.
Product
Gender Solutions" Natural-Knee¿ Flex System: N-K FLEX MBACK SZ 0 PAT N-K FLEX MBACK SZ 1 PAT N-K FLEX MBACK SZ 2 PAT
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1226-2014·2014-03-26
Ortho-Clinical VITROS White Correction Factor Slides Recalled for Labeling Error
Ortho-Clinical Diagnostics is recalling VITROS White Correction Factor Slides because an incorrect assay value was printed on the carton, which may delay reporting of specific test results.
Product
VITROS Chemistry Products White Reference Slides, White Correction Factor Slide (WCF), DT Slides, 25 Slides, Part Number J02315; Made in USA by Ortho- Clinical Diagnostics, Inc. 100 Indigo Creek Drive, Rochester, NY 14626 --- This product is a part/ tool used when performing the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1254-2014·2014-03-26
Zimmer Recalls Natural-Knee Tibial Inserts Due to Discoloration
Zimmer, Inc. is recalling 3,638 Natural-Knee Congruent Tibial Inserts with Screws because a complaint identified discoloration caused by premature oxidation during storage.
Product
Natural-Knee¿ Congruent Tibial Insert with Screw: SF-CON TIB INS LT SZ1/2 1 SF-CON TIB INS RT SZ1/2 9 SF-CON TIB INS RT SZ3/4/5
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1166-2014·2014-03-26
Pfizer Recalls Advil PM Caplets Due to Low Diphenhydramine Levels
Pfizer is recalling 70,704 bottles of Advil PM caplets nationwide because the diphenhydramine citrate content was found to be out of specification.
Product
ADVIL PM — ADVIL PM (DIPHENHYDRAMINE CITRATE AND IBUPROFEN)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1167-2014·2014-03-26
McKesson Recalls Venlafaxine Hydrochloride Capsules for Dissolution Failure
McKesson Packaging Services is recalling 1,557 boxes of Venlafaxine Hydrochloride Extended Release Capsules, 150 mg, due to out-of-specification dissolution results.
Product
Venlafaxine Hydrochloride, Extended Release Capsules, 150 mg, UD-100 Tablets per Box (10 x 10), Rx Only, Manufactured by: Teva Pharmaceuticals USA, 1090 Horsham Rd, North Wales, PA 19454, NDC 63739-0512-10
Category
Drug
Distribution
Distributed nationwide
SevereCPSC·14138·2014-03-25
Centex Homes Recalls SolarSave Roof Panels Due to Fire Hazard
Centex Homes is recalling SolarSave roof panels installed on new homes due to a fire hazard. Two roof fires have been reported, with no injuries.
Product
SolarSave® roof panels
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·14V143000·2014-03-25
NABI Transit Buses Recalled for CNG Fuel Cylinder Interference Risk
NABI is recalling 2013-2014 transit buses equipped with compressed natural gas systems because a bolt may damage the fuel cylinder, posing a fire risk.
Product
NABI — NABI 40LFW, 35LFW, 31LFW
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·14140·2014-03-25
Wal-Mart Recalls Electronic Baby Dolls Due to Burn Hazard
Wal-Mart is recalling My Sweet Love and My Sweet Baby Cuddle Care dolls because the internal circuit board can overheat, posing a burn risk to consumers.
Product
My Sweet Love / My Sweet Baby Cuddle Care Baby Doll
Category
Consumer Product
Distribution
Distributed nationwide