Recalls distributed in New Mexico
These notices name New Mexico in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.
1,959 stored notices name New Mexico, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach New Mexico too — those are in the archive.
Reported Sep 18, 2019
PediaSmart Organic Soy Vanilla Beverage Mix, 12.7 oz. (360g) composite can
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natures One Inc.
FDA (openFDA food enforcement)
Reported Sep 18, 2019
XP- CR Tibial Tray- Interlok 59mm Item # 195268
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
34 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 11, 2019
Alere Cholestech LDX Analyzer, model # 14-874 containing power supplies with the identifying codes of 1837d and 1843d -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alere San Diego, Inc.
FDA (openFDA device enforcement)
Reported Sep 11, 2019
Norm-O-Temp model 111Z
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cincinnati Sub-Zero Products LLC, a Gentherm Company
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 11, 2019
Flexible Intubation Fiberscope, Model # 11301AB1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
FDA (openFDA device enforcement)
Reported Sep 4, 2019
EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER, REF/Product Code:5905190, 14.5 Fr. Alphacurve Catheter with Standard Kit,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
27 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 28, 2019
Kit BD Max Check-Points CPO IVD EU; Catalog # 278102
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
18 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 28, 2019
DeRoyal Enteral Safe Feeding Tubes: a) REF 54-2450R, 5 FR x 24" Polyurethane b) REF 54-2465R, 6.5 FR x 24" Polyurethane…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DeRoyal Industries Inc.
FDA (openFDA device enforcement)
Reported Aug 28, 2019
ACUSON NX2 Diagnostic Ultrasound System, Model # 11284381, RX Only, Siemens Medical Solutions, containing software…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 28, 2019
PRIVATE SELECTION FROZEN TRIPLE BERRY MEDLEY, 48 oz
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Kroger Co.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 28, 2019
Kirkland Signature Three Berry Blend product, frozen, package in a plastic bag. Net wt. 4 lbs. UPC 0 96619 10105 4. The…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Townsend Farms Inc.
FDA (openFDA food enforcement)
Reported Aug 21, 2019
iGUIDE System with software build iGuide 2.2.0, 2.2.1, and 2.2.2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Aug 21, 2019
Aries Bordetella Assay, REF 50-10037, UDI # 00840487101452
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Corporation
6 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 21, 2019
Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151810
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 14, 2019
Endoscopic Cleaning Brushes sold in various Endoscopy Kits - Product Usage: The brushes are used to help clean out the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
FDA (openFDA device enforcement)
Reported Aug 14, 2019
Ginger Spice, 1 oz (28.4 g), 2 oz, 4 oz, and 1-3 lb packages. An herbal tea, Taos, NM
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Milkweed & Monarch, LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 7, 2019
Maximum Pelvic Trainer (MPT)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ralston Group
FDA (openFDA device enforcement)
Reported Jul 31, 2019
Breast Milk Transfer Lid for use with Oral Syringe Connectors Model: 90003S-100
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Medela Inc.
FDA (openFDA device enforcement)
Reported Jul 31, 2019
Ragu Chunky Sauce Tomato, Garlic & Onion 45oz and 66oz retail sizes sold in plastic jars
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mizkan America, Inc. - Corporate
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 31, 2019
ACID RAIN ASS KICKING FAT DESTROYER APOCALYPSE LABZ; 45 CAPSULES; 1 DIETARY SUPPLEMENT; UPC 6 11138 28792 0
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nexagen, LLC
FDA (openFDA food enforcement)
Reported Jul 24, 2019
TAPSYSTEM Model 2A, REF 8002A
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Cardiocommand Inc.
FDA (openFDA device enforcement)
Reported Jul 24, 2019
Alaris Pump, Model 8100, with bezel mechanical assemblies manufactured with FR-110 plastic resin. The following…
High riskUsing this product could cause serious injury, illness or death — stop using it now.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Jul 24, 2019
Lay' Lightly Salted Barbecue Flavored Potato Chips Net Wt. 7 3/4 OZ. UPC Code 2840063242
High riskUsing this product could cause serious injury, illness or death — stop using it now.Frito-Lay, Inc.
FDA (openFDA food enforcement)
Reported Jul 24, 2019
Anti-fog solution packaged in a Tyvek peel pouch and it is placed into various kits. Kit are labeled as follows:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries, Inc.
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new New Mexico recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
Other states
RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.