All recall categories

Recalls distributed in Maine

These notices name Maine 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.

1,801 stored notices name Maine, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Maine too — those are in the archive.

Medical devices

Reported Sep 22, 2021

Arjo Disposable Repositioning Sling, Model AHD001

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Getinge Dominican Republic SA

FDA (openFDA device enforcement)

Medical devices

Reported Sep 22, 2021

Potassium Hydroxide 10% (KOH 10%), Cat. No. 300145 Potassium Hydroxide 10% (KOH 10%) is intended for use in the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Gibson Bioscience

FDA (openFDA device enforcement)

Food

Reported Sep 22, 2021

Jimbo's BLOODY MARY MIX; 2.5OZ MAKES ABOUT 45 SERVINGS; Ingredients: Horseradish Powder, Parsley, Worcestershire…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Jimbo's Kitchen

FDA (openFDA food enforcement)

Medical devices

Reported Sep 15, 2021

Pipeline Flex Embolization Device

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Micro Therapeutics Inc.,

1 more product in this recall

FDA (openFDA device enforcement)

Drugs

Reported Sep 15, 2021

QiYu Hand Sanitizer (ethyl alcohol 75% (v/v)), 16.9 FL OZ (500 ML) bottles, Manufactured by: Guangzhou Minghui…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Native Promotions, Inc.

FDA (openFDA drug enforcement)

Food

Reported Sep 8, 2021

Hostess Soft White Hamburger Buns, Net Wt. 12 OZ, UPC 888109110987

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hostess Brands, LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 1, 2021

Monoject 0.9% Sodium Chloride Flush Syringe, 10 mL Fill, STERILE, Product Code 8881570121 The proposed device is…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Cardinal Health

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 1, 2021

AltiVate Anatomic Shoulder System for the following Part Numbers: 1. Part # 520-08-00, Rev. C., 2. Part # 520-10-000,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Encore Medical, LP

FDA (openFDA device enforcement)

Medical devices

Reported Sep 1, 2021

Gore Molding & Occlusion Balloon Catheter, REF Catalogue Number MOB37, SN XXXXXXXX, 10 mm - 37 m 10 Fr, Guidewire…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

W. L. Gore & Associates Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 25, 2021

OPTI SARS-CoV-2 RT-PCR Test, REF Numbers: a) 99-57003 b) 99-57004

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

OPTI Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 25, 2021

EPIQ Ultrasound Systems, Model: EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 5W, EPIQ 7G, EPIQ 7C, EPIQ 7W, EPIQ CVx, EPIQ CVxi

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Ultrasound Inc.

FDA (openFDA device enforcement)

Meat & poultry

Reported Aug 24, 2021

Willow Tree Poultry Farm Recalls Chicken Salad and Dip Products Due to Possible Foreign Matter Contamination

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Willow Tree Poultry Farm, Inc.

USDA FSIS

Medical devices

Reported Aug 18, 2021

ACCESS SARS-CoV-2 Antigen , REF: C68668, IVD, Rx only, UDI: (01) 15099590742713;

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beckman Coulter Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 18, 2021

Kaluza C Flow Cytometry Software Versions: 1.0*, 1.1.1 and 1.1.2 Kits: C10574 - Kaluza C Single Perpetual License…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beckman Coulter, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 18, 2021

ETEST IMIPENEM RELEBACTAM. in vitro diagnostic

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Biomerieux Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 18, 2021

Chassis Label - "CIRRUS HD-OCT Rx-Only" Product Label Exterior RX - "CIRRUS HD-OCT Model 6000"

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Carl Zeiss Meditec, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 18, 2021

Solumeve Hydrolyzed Collagen Peptides, Turmeric + MCT and Ginger; Dietary Supplement, NET Wt. 14.1 oz. (400g) Suggested…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Iherb LLC

FDA (openFDA food enforcement)

Food

Reported Aug 18, 2021

Wickles Relish 16oz glass jars - 6 jars per case

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Magnolia Vegetable Processors

FDA (openFDA food enforcement)

Medical devices

Reported Aug 18, 2021

Medtronic StimLoc Burr Hole Cover, Part Numbers: a) 3387S-40 b) 3389S-28 c) 3389S-40 d) 3391S-40 e) 3550S-01 f) 924256…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Neuromodulation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 18, 2021

Prelude SNAP Splittable Sheath Introducer, REF: PLSX -1010, size 10F, Standard Length: 13 cm, CE0344, STERILE EO, Rx…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Merit Medical Systems, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 18, 2021

Monfefo brand Turmeric Shot; 2oz; Cold Pressed Juice Blend; packaged in glass bottle

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Monfefo LLC

FDA (openFDA food enforcement)

Medical devices

Reported Aug 11, 2021

REF: 08P1820, Abbott Alinity c Activated Alanine Aminotransferase reagent Kit, Alinity c Activated Alanine…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Laboratories

3 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported Aug 11, 2021

Global Hand Sanitizer with moisturizer, Alcohol-based Antiseptic 80%, Non-sterile Topical Solution, 4 fl. oz./119 mL,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cascade Kelly Holdings LLC

1 more product in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Aug 11, 2021

GlideScope Go Monitors

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Verathon, Inc.

FDA (openFDA device enforcement)

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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.