State

New Mexico product recalls

73,092 recalls have nationwide distribution and so reach New Mexico. 3,628 additional recalls listed New Mexico specifically in their distribution scope.

What the numbers show

Total: 3,628
Critical: 747
Severe: 649
Most recent: 2026-09-23

Of the 3,628 recalls naming New Mexico we have scored against our rubric, 747 (21%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 649 (18%) are Severe.

Which agencies issued them

These figures cover only the 3,628 recalls whose distribution notice names New Mexico specifically. The 73,092 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

7251–7275 of 76720

SevereFDA (Devices)·Z-1494-2025·2025-04-09
Draeger ID Circuit Flex 220 breathing circuit hoses subject to cracking
Draeger's ID Circuit Flex 220 breathing circuit for anesthesia machines may develop cracks in the hose. The recall affects 3,325 units distributed nationwide and internationally.
Product
Brand Name: ID Circuit Product Name: ID Circuit Flex 220 Model/Catalog Number: MP01347 Software Version: Not applicable Product Description: Breathing circuit for conveying breathing gases between an anesthesia machine or ventilator and adult Component: Not applicable
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1499-2025·2025-04-09
Anesthesia Circuit Kit Flex EPA recalled due to breathing hose cracking
Draeger is recalling the Anesthesia Circuit Kit Flex EPA due to the potential for cracks to form in the breathing circuit hose. Approximately 13,620 units have been distributed domestically and internationally. Users should discontinue use of affected units immediately.
Product
Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex EPA Model/Catalog Number: MP17103 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intend
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1493-2025·2025-04-09
VentStar Flex 220 Breathing Circuit Recalled for Potential Hose Cracks
Draeger, Inc. is recalling 65,150 units of the VentStar Flex 220 breathing circuit due to the potential for cracks to form in the hose. A crack could affect gas delivery during anesthesia or ventilation procedures.
Product
Brand Name: VentStar Product Name: VentStar Flex 220 Model/Catalog Number: MP00355 Software Version: Not applicable Product Description: Breathing circuit for conveying breathing gases between an anesthesia machine or ventilator and adult patients. The breathing circuit is in
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1497-2025·2025-04-09
Anesthesia Circuit Kit Flex 6 Recalled for Potential Breathing Hose Cracks
Draeger, Inc. is recalling the Anesthesia Circuit Kit Flex 6 (Model MP02744) due to potential cracks forming in the breathing circuit hose. Approximately 293,660 units were distributed nationwide and internationally.
Product
Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 6 Model/Catalog Number: MP02744 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intended
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0308-2025·2025-04-09
Prescription Duloxetine Capsules Recalled for Nitrosamine Impurity
Breckenridge Pharmaceutical is recalling Duloxetine 30 mg capsules distributed nationwide due to a nitrosamine impurity above acceptable limits. Consumers should consult their doctor about their medication.
Product
DULOXETINE — DULOXETINE (DULOXETINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0693-2025·2025-04-09
Good & Gather Baby Vegetable Puree Recalled for Elevated Lead Levels
Good & Gather baby vegetable puree (4 oz) is being recalled due to elevated levels of lead. The recall affects 25,600 units distributed nationwide by Target.
Product
Good & Gather baby Pea, Zucchini, Kale & Thyme Vegetable Puree. Net Wt 4 oz. (113g). 6+ months. UPC 1 91907-99314 1. Distributed by Target Corporation, Minneapolis, MN 55403. Product of Colombia
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1500-2025·2025-04-09
Phoroptor VRx Digital Refraction System head may become loose or detach
Reichert, Inc. is recalling 122 units of the Phoroptor VRx Digital Refraction System Model 16241 due to an assembly defect that could cause the device head to become loose and potentially detach.
Product
Phoroptor VRx Digital Refraction System Model Numbers: 16241
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1471-2025·2025-04-09
Nasopore Standard Nasal Dressing Recalled Due to Sterility Seal Defects
Stryker is recalling 182,344 units of Nasopore Standard nasal dressings nationwide due to potential bubbles in blister seals that may breach the sterility barrier and increase contamination risk.
Product
Nasopore Standard 8cm fragmentable nasal dressing, Catalog Numbers 5400-010-008 and 5400-010-008ITL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1482-2025·2025-04-09
Stryker nasal wound dressing recalled for defective sterile packaging seal
Stryker Corporation is recalling 182,344 units of Hemopore 2PK nasal/sinus wound dressing due to potential bubbles in blister seals that indicate sterility breach. Affected lot numbers are 2024020221, 2024051720, and 2024082321.
Product
Hemopore 2PK nasal/sinus temporary wound dressing, Catalog Number 5400-222-208S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1475-2025·2025-04-09
Otopore Square Outer Ear Wound Dressing Recall for Sterility Seal Defect
Stryker Corporation is recalling Otopore Square outer ear wound dressings nationwide because sterile packaging seals may develop bubbles, indicating a potential breach of the sterile barrier. Consumers should stop using affected units and contact their healthcare provider.
Product
Otopore Square outer ear wound dressing, Firm Catalog Number 5400-020-100 and Forte Catalog Number 5400-020-100ITL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1477-2025·2025-04-09
Hemopore nasal wound dressing packaging seal defect may compromise sterility
Stryker Corporation is recalling 182,344 units of Hemopore nasal/sinus wound dressing due to potential packaging seal defects that could compromise sterility. A bubble on the blister seal may indicate the sterile barrier has been breached.
Product
Hemopore 8cm nasal/sinus temporary wound dressing, Catalog Numbers 5400-020-208 and 5400-020-208ITL (OUS)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1501-2025·2025-04-09
Phoroptor VRx Digital Refraction System Recalled for Detachable Head
Reichert is recalling 1,876 units of the Phoroptor VRx Digital Refraction System (Model 16242) due to an assembly defect that could cause the refraction head to detach during eye examinations.
Product
Phoroptor VRx Digital Refraction System Model Numbers: 16242
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25E025000·2025-04-09
Hiab Recalls Waltco ZS-MK2 Lift Gates Due to Pin Seizure Risk
Hiab USA Inc. is recalling specific Waltco ZS-MK2 series lift gates because insufficient lubrication may cause the cylinder pin to seize, leading to lift gate failure and injury risk.
Product
STRUCTURE:BODY:HATCHBACK/LIFTGATE recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25C005000·2025-04-09
Chicco Recalls MyFit Zip Air Harness and Booster Child Seats
Chicco is recalling specific MyFit Zip Air Harness and Booster child seats because they may allow excessive chest movement in a crash, increasing injury risk.
Product
CHILD SEAT recall
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·25V225000·2025-04-09
Audi Q6 e-tron rearview cameras may show a blurry image
Volkswagen is recalling certain 2025 Audi Q6 e-tron and SQ6 e-tron vehicles because the rearview camera may show a blurry image, failing FMVSS 111.
Product
AUDI — AUDI Q6 E-TRON, SQ6 SPORTBACK E-TRON
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1516-2025·2025-04-09
Surgical Suture Recall Due to Silicone Curing Defect
Ethicon Endo Surgery recalls ETHIBOND EXCEL surgical sutures worldwide due to curing issues with the silicone coating on the needles identified during manufacturing.
Product
ETHIBOND EXCEL GRN 36IN(90CM) USP2-0(M3) D/A MH
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1481-2025·2025-04-09
Nasopore Nasal Dressings Recalled Due to Breached Sterility Seals
Stryker Corporation is recalling Nasopore nasal dressings due to potential breaches in packaging sterility seals that could compromise product sterilization. Approximately 182,344 units have been distributed nationwide.
Product
Nasopore 4cm Standard 2PK fragmentable nasal dressing, Catalog Number 5400-212-004S and Nasopore 4cm Firm 2PK Catalog Number 5400-222-004S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0684-2025·2025-04-09
SeaBear Salmon Chowder Recalled for Potential Seal Failure and Botulinum Risk
SeaBear Smokedhouse Salmon Chowder is recalled due to potential seal failure that could allow Clostridium botulinum contamination. The recall affects 11,152 pouches distributed nationwide.
Product
SeaBear Smokedhouse Salmon Chowder is packaged in flexible retort pouch, net wt. 12-oz., UPC 0 34507 07001 3. Case label: Item 60077 Salmon Chowder 12/12oz, SeaBear/G&D Anacortes, WA.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1515-2025·2025-04-09
Ethicon PROLENE BLU Surgical Sutures Recalled for Manufacturing Defect
Ethicon is recalling specific lots of PROLENE BLU surgical sutures due to silicone curing issues during needle manufacturing.
Product
PROLENE BLU 18IN(45CM) USP6-0(M0.7) S/A P-1 PRM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1472-2025·2025-04-09
Otopore Cylinder Wound Dressing Recalled for Potential Sterility Seal Defect
Stryker Corporation recalls Otopore Cylinder outer ear wound dressing due to potential bubbles in blister seals that may breach the sterile barrier. Affected units were distributed nationwide.
Product
Otopore Cylinder outer ear wound dressing, Firm Catalog Number 5400-020-000 and Forte Catalog Number 5400-020-000TL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0685-2025·2025-04-09
SeaBear Clam Chowder Recalled for Potential Botulinum Contamination
SeaBear Smokedhouse Alehouse Clam Chowder pouches are recalled nationwide due to potential seal failure that could allow Clostridium botulinum contamination. Consumers should not consume the product.
Product
SeaBear Smokedhouse Alehouse Clam Chowder is packaged in retort pouch, net wt. 12-oz., UPC 0 34507 07021 1. Case label, item 60104, Alehouse Chowder 12/CS.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1480-2025·2025-04-09
Nasopore Nasal Dressing Recall Due to Compromised Sterile Packaging Seals
Stryker Corporation is recalling Nasopore nasal dressings due to potentially compromised sterile packaging seals. Affected units totaling 182,344 may have lost sterility, posing a contamination risk.
Product
Nasopore 4cm Standard 2PK fragmentable nasal dressing, Catalog Number 5400-212-004S and Nasopore 4cm Firm 2PK Catalog Number 5400-222-004S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1476-2025·2025-04-09
Nasopore FD nasal dressing recalled for potential sterile barrier breach
Stryker Corporation is recalling 182,344 units of Nasopore FD nasal dressing nationwide due to potentially breached sterile seals that may allow product contamination.
Product
Nasopore FD fragmentable nasal dressing, Catalog Numbers 5400-020-108 and 5400-020-108ITL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1473-2025·2025-04-09
Stryker Nasopore Nasal Dressing Recalled for Compromised Sterility Seals
Stryker's Nasopore 8cm nasal dressing is being recalled because packaging seals may have bubbles indicating the sterility barrier has been breached. The recall affects 182,344 units distributed nationwide.
Product
Nasopore 8cm fragmentable nasal dressing, Firm Catalog Number 5400-020-008 and Forte Catalog Number 5400-020-008ITL
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V226000·2025-04-09
Audi Q6 rearview camera image may be delayed or deactivated
Volkswagen is recalling certain 2025 Audi Q6 and SQ6 vehicles because the rearview camera image may be delayed or deactivated after shifting into reverse, failing FMVSS 111.
Product
AUDI — AUDI SQ6 SPORTBACK E-TRON, Q6 E-TRON
Category
Vehicle
Distribution
Distributed nationwide