State

Northern Mariana Islands product recalls

72,820 recalls have nationwide distribution and so reach Northern Mariana Islands. 22 additional recalls listed Northern Mariana Islands specifically in their distribution scope.

What the numbers show

Total: 22
Critical: 0
Severe: 8
Most recent: 2025-02-05

Of the 22 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 8 (36%) are Severe.

Which agencies issued them

These figures cover only the 22 recalls whose distribution notice names Northern Mariana Islands specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

901–925 of 72842

SevereFDA (Food)·H-1098-2026·2026-07-01
Spring & Mulberry Earl Grey Date-Sweetened Chocolate Bars Recalled
Spring & Mulberry Inc. is recalling Earl Grey Date-Sweetened Chocolate bars due to potential Salmonella contamination. The affected product was distributed nationwide.
Product
Spring & Mulberry Earl Grey Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a purple box, UPC 850055470231, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold indivi
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2583-2026·2026-07-01
Medical Device Surgical Kits with Syringes Recalled for Unapproved Design Changes
Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes used in surgical procedures. The manufacturer identified unapproved design changes to the products that were not cleared by the FDA through the 510(k) process.
Product
Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. BARIATRIC DYNJ905153J DYNJ905153K DYNJ905153L GYNE LAPAROTOMY PACK-LF DYNJ49593A LAPAROSCOPY DYNJ905157G DYNJ905157I DYNJ905157J LAPAROSCOPY PACK DYNJ56930B MAJOR PLUS
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2453-2026·2026-07-01
Medline Convenience Kits with Lidocaine and Bupivacaine Injections Recalled
Medline Industries is recalling 22 models of Convenience Kits that contain Lidocaine Hydrochloride Injection and Bupivacaine Hydrochloride in Dextrose Injection due to quality issues found during an FDA inspection of the supplier.
Product
Medline Convenience Kits: 1) OPEN HEART CDS, Model Number: CDS840144Q; 2) OPEN HEART, Model Number: CDS840150W; 3) OPEN HEART ADULT, Model Number: CDS840396AA; 4) CABG A CDS, Model Number: CDS982269N; 5) OPEN HEART ANESTHESIA PACK, Model Number: CDS983849G; 6) OPEN HE
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-1102-2026·2026-07-01
Spring & Mulberry Pecan Date Chocolate Recalled for Salmonella Risk
Spring & Mulberry Inc. is recalling approximately 79,156 individually packaged pecan date date-sweetened chocolate bars nationwide due to potential Salmonella contamination.
Product
Spring & Mulberry Pecan Date Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a yellow box, UPC 850055470040, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold indiv
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·H-1106-2026·2026-07-01
Spring & Mulberry Blood Orange Date-Sweetened Chocolate recalled for Salmonella
Spring & Mulberry Inc. is recalling Blood Orange Date-Sweetened Chocolate bars due to potential Salmonella contamination. Affected products were distributed nationwide.
Product
Spring & Mulberry Blood Orange Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in an orange box, UPC 850055470200, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold in
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0625-2026·2026-07-01
ChloraPrep One-Step Antiseptic Solution Recall Due to Sterility Concerns
CareFusion is recalling 178,000 ChloraPrep One-Step antiseptic applicators (Lot #4073005) nationwide due to potential non-sterility from fungal contamination and seal breaches from paper lidding wrinkles.
Product
CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0626-2026·2026-07-01
Lacosamide 100mg Tablets Recalled Due to Foreign Tablet Contamination
Annora Pharma is recalling Lacosamide 100mg tablets nationwide after discovering Selexipag 1000 mcg tablets mixed into bottles. Patients taking the wrong medication could experience unintended health effects.
Product
LACOSAMIDE — LACOSAMIDE (LACOSAMIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-1095-2026·2026-07-01
Motor City Pizza Co. 5 Cheese Bread recalled for salmonella risk
Champion Foods, LLC is recalling Motor City Pizza Co. 5 Cheese Bread due to potential salmonella contamination. Affected products were distributed nationwide at major retailers.
Product
Motor City Pizza Co. 5 Cheese Bread Single retail pack; 22.43 oz. (1 lb. 6.4 oz.) 636g UPC 8 70375 00511 1; 6 retail units per case Motor City Pizza Co. 5 Cheese Bread Twin retail pack; 44.86 oz. (2 lb. 12.9 oz.) 1272g UPC 8 70375 00509 8; 10 retail units per case
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2567-2026·2026-07-01
Surgify Halo surgical burrs recalled for potential breakage
Surgify Halo 5.4 mm Short surgical burrs may break during bi-portal endoscopic spinal surgery. FDA Class II recall affects multiple U.S. states.
Product
Surgify Halo, 5.4 mm, Short, Model/Catalog Number: 54.070.NVG.U1; drills, burrs, trephines & accessories (simple, powered)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2568-2026·2026-07-01
Surgify Halo Surgical Burr Breakage Risk During Spinal Surgery
Surgify Medical is recalling Surgify Halo 5.4 mm Medium surgical burrs due to potential burr breakage during bi-portal endoscopic spinal surgery. The device poses a risk of fragmentation that could complicate surgical procedures.
Product
Surgify Halo, 5.4 mm, Medium, Model/Catalog Number: 54.085.SHD.H1; burrs, trephines & accessories (simple, powered)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2532-2026·2026-07-01
Acumed Hexalob Screws Recalled for Risk of Fracture During Use
Acumed LLC is recalling Hexalob Screws of various sizes used with wrist fixation systems due to a manufacturing error that may cause the screws to break during use.
Product
Acumed Hexalob Screw various sizes: REF Numbers: : 3070-27008 2.7mm x 8mm NL Hexalobe Screw; 3070-27009 2.7mm x 9mm NL Hexalobe Screw; 3070-27010 2.7mm x 10mm NL Hexalobe Screw; 3070-27011 2.7mm x 11mm NL Hexalobe Screw; 3070-27012 2.7mm x 12mm NL Hexalobe Screw; 3070-27013
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2586-2026·2026-07-01
Medline Industries Polycarbonate Syringes Convenience Kits Design Change Recall
Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside of FDA 510(k) clearance. Affected kits were distributed nationwide and internationally.
Product
Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ANGIOGRAPHY PACK-LF DYNJ0854485S DEEP BRAIN STIMULATION PACK DYNJ0842793G NEURO ACCESSORY PACK DYNJ55385A NEURO ANGIO PACK DYNJ51697B DYNJ56509G DYNJ56509I DYNJ680
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2560-2026·2026-07-01
Surgify Halo surgical burr recalled for potential breakage risk
Surgify Medical is recalling the Surgify Halo 4.0 mm surgical burr because it may break during bi-portal endoscopic spinal surgery. The device is distributed nationwide.
Product
Surgify Halo, 4.0 mm, Short, Model/Catalog Number: 40.070.NVG.H1; drills, burrs, trephines & accessories (simple, powered)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2570-2026·2026-07-01
Surgify Halo surgical burrs recalled for potential breakage risk
Surgify Medical is recalling the Surgify Halo 5.4 mm surgical burrs due to potential breakage during spinal surgery procedures.
Product
Surgify Halo, 5.4 mm, Long, Model/Catalog Number: 54.125.NVG.H1; drills, burrs, trephines & accessories (simple, powered)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2564-2026·2026-07-01
Surgify Halo Surgical Burrs Recalled Due to Breakage Risk
SURGIFY MEDICAL OY is recalling Surgify Halo 5.4 mm Extendable surgical burrs (Model 54.000.SEE.H1) due to potential for burr breakage during bi-portal endoscopic spinal surgery. The device has been distributed nationwide.
Product
Surgify Halo, 5.4 mm, Extendable, Model/Catalog Number: 54.000.SEE.H1; drills, burrs, trephines & accessories (simple, powered)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2566-2026·2026-07-01
Surgify Halo Spinal Surgery Burrs Recalled for Breakage Risk
Surgify Medical is recalling Surgify Halo 5.4 mm Short burrs (Model 54.070.NVG.H1) due to potential breakage during bi-portal endoscopic spinal surgery. The hazard could affect patient safety during the procedure.
Product
Surgify Halo, 5.4 mm, Short, Model/Catalog Number: 54.070.NVG.H1; drills, burrs, trephines & accessories (simple, powered)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2580-2026·2026-07-01
Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump recall
Boston Scientific Corporation is recalling the Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump (model AP-0300H) due to potential leakage along the drug pathway from the pump through the catheter.
Product
Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump, AP-0300H, implantable drug delivery device
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2562-2026·2026-07-01
Surgify Halo surgical drill may break during spinal surgery procedures
Surgify Halo 4.0 mm surgical drills are being recalled because the burr may break during bi-portal endoscopic spinal surgery. The defect could interfere with the surgical procedure.
Product
Surgify Halo, 4.0 mm, Short, Model/Catalog Number: 40.125.NVG.H1; drills, burrs, trephines & accessories (simple, powered)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2569-2026·2026-07-01
Surgify Halo Surgical Burrs Subject to Potential Breakage Recall
Surgify Halo 5.4 mm surgical burrs may break during bi-portal endoscopic spinal surgery. The FDA has classified this as a Class II recall affecting devices distributed nationwide.
Product
Surgify Halo, 5.4 mm, Medium, Model/Catalog Number: 54.085.SHD.U1; drills, burrs, trephines & accessories (simple, powered)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2524-2026·2026-07-01
TMJ Bilateral Implants with Incorrect Patient-Specific Components Recalled
TMJ Solutions Inc is recalling TMJ Bilateral Implants (REF: CHG020) because some units may contain incorrect patient-specific components, causing poor implant fit and right-sided open bite.
Product
TMJ Bilateral Implants, REF: CHG020
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2552-2026·2026-07-01
Stryker Neurovascular INZONE Detachment System battery drain
Stryker Neurovascular is recalling the INZONE Detachment System (REF: M00345100950) due to premature battery drain that may prevent the device from powering on or detaching coils as intended.
Product
INZONE DETACHMENT SYSTEM, REF: M00345100950
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2528-2026·2026-07-01
Zimmer Shoulder Reamer Guide System Recalled for Plastic Breakage
Zimmer is recalling Off-Axis Comprehensive Shoulder System reamer guides (Model 110040241) because plastic guides can catch and break during reaming. Five complaints have been received.
Product
Off-Axis Comprehensive Shoulder System, Medium, Augment, Off-Axis, Reamer Guide Model/Catalog Number: 110040241
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2561-2026·2026-07-01
Surgify Halo 4.0 mm Spinal Surgery Burrs May Break During Use
Surgify Halo 4.0 mm Short burrs may break during bi-portal endoscopic spinal surgery, creating a potential hazard during the procedure. The FDA has classified this as a Class II recall affecting devices nationwide.
Product
Surgify Halo, 4.0 mm, Short, Model/Catalog Number: 40.070.NVG.U1; drills, burrs, trephines & accessories (simple, powered)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2555-2026·2026-07-01
Surgify Halo Surgical Burr Potential Breakage During Endoscopic Spinal Surgery
Surgify Medical is recalling Surgify Halo 3.0 mm Extendable surgical burrs because they may break during bi-portal endoscopic spinal surgery, posing a risk to patients.
Product
Surgify Halo, 3.0 mm, Extendable, Model/Catalog Number: 30.000.SEE.U2; drills, burrs, trephines & accessories (simple, powered)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2553-2026·2026-07-01
GE Healthcare AW Server Radiological Image Processing System Software Defect
GE Healthcare is recalling the AW Server 3.2 ext. 6.5 radiological image processing system due to a software synchronization issue that may cause the wrong patient's images to be displayed without warning, potentially leading to misdiagnosis.
Product
GE Healthcare AW Server 3.2 ext.6.5; Radiological Image Processing System
Category
Medical Device
Distribution
Distributed nationwide