All recall categories

Recalls distributed in Maryland

These notices name Maryland 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.

4,061 stored notices name Maryland, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach Maryland too — those are in the archive.

Medical devices

Reported Apr 4, 2018

(1) Sigma HP Cemented Trochlea Size 1 Narrow Left, Catalog Number: 102403100, GTIN: 10603295001614; (2) Sigma HP…

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

DePuy Orthopaedics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 4, 2018

Sonimage HS1 Ultrasound Kit AC adapter, Product Number: A7AP, UDI: 04560141940031

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

Konica Minolta Medical Imaging USA, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 4, 2018

Gas Module 3 monitoring spirometer, Part Number: 115-030108-00 Product Usage: The Gas Module 3 is an accessory device…

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

Mindray DS USA, Inc. dba Mindray North America

FDA (openFDA device enforcement)

Food

Reported Apr 4, 2018

Wegmans Thai Sweet Chili Sauce Cup 1.5 oz. (UPC 7-66630-98023)

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

Wegmans Food Markets, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 4, 2018

Zimmer M/L Taper Hip Prosthesis, 7711 Series, Femoral Stem 12/14 Neck Taper Plasma Sprayed Press-Fit Cementless Size…

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

Zimmer Biomet, Inc.

19 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 28, 2018

BD Vacutainer¿ EDTA Lavender Top Tubes: Catalog Numbers: 1. 366401 (UDI: 50382903664011); 2. 366450 (UDI:…

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

Becton Dickinson & Company

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 28, 2018

Malecot Nephrostomy Catheter System, Product Number: M001224110, GTIN: 08714729030980 The Malecot and the Stenting…

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

Boston Scientific Corporation

6 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 28, 2018

Name: Trader Joe s Chocolate Chip Cookies SKU 68075 Net Weight: 12 oz. (340g) Number of units per package: 16 cookies…

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

Food and Beverage Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 28, 2018

CATHETER REPAIR KIT, REF AAC52001, UDI 884908001891 Product Usage: The Medcomp Repair Kit is indicated for use in…

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

Medical Components, Inc. dba MedComp

9 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 28, 2018

ClariVein IC infusion catheter, Model Number: 65-018-E4S Product Usage: The ClariVein IC infusion catheter is indicated…

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

Vascular Insights, LLC

FDA (openFDA device enforcement)

Food

Reported Mar 28, 2018

Weis Sunbury, PA 17801; Penne W/Asiago Sauce And Grilled Chix Small Meal; multiple weight. SCALE UPC - 205377-00000

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

Weis Markets

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 21, 2018

NovaKone Daily Wear Soft contact; Catalog Number: AONKS54 Product Usage: The NOVAKONE SPHERICAL lens is indicated for…

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

Alden Optical

10 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 21, 2018

Difco" Agar Noble, 500g bottle Noble Agar is a solidifying agent that is essentially free of impurities. It is used in…

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

Becton Dickinson & Co.

FDA (openFDA device enforcement)

Food

Reported Mar 21, 2018

Kodiak Cakes, Energy Waffles, Blueberry Chia, Net Wt 10.72 Oz (304 g), Kodiak Cakes, Park City, UT. Packaging…

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

Kodiak Cakes, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Mar 21, 2018

OneStep CPR Complete, Adult Multi Function Electrodes, Part Numbers: 8900 0214 01 (case of 8 single electrodes, UDI:…

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

ZOLL Medical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 14, 2018

i-STAT DE handheld data processing module for clinical use, Software Version 2.8, List Number:08K46-01115200 (UDI:…

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

Abbott Point Of Care Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 14, 2018

O-arm¿ O2 interventional fluoroscopic x-ray system; Catalog Number: B1-700-02000 The O-arm O2 Imaging System is a…

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

Medtronic Navigation, Inc.-Littleton

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 14, 2018

Medtronic Synchromed II Model 8637 supplied in 20mL and 40 mL reservoir size and a catheter. Product Usage: The…

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

Medtronic Neuromodulation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 14, 2018

cobas 6000 Modular Series system; Part Numbers: 1. 04745914001 cobas c 501 module; 2. 05036453001 cobas 6000 UL c 501 +…

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

Roche Diagnostics Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 14, 2018

Springside Monterey Jack Garden Vegetable Cheese, 40 lbs.

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

Springside Cheese Corp.

11 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 14, 2018

2.5 mm Reaming Rod, Ball tip, 950 mm, sterile, Part Number: 351.706S Reaming Rods are intended for guiding of reamers…

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

Synthes (USA) Products LLC

6 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 14, 2018

Product packaged in the following ways A) Sonne's, No. 17, Natural Source Vitamin C, Dietary Supplement, (920 mg tablet…

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

Vitalab Co. Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 14, 2018

Flexible Shaft hip and anatomical shoulder instrument used for preparation of bone in Trauma, Hip and Shoulder…

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

Zimmer Biomet, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 7, 2018

Soft-Vu Omni Flush Angiographic Catheter (UPN H787107322015); SV OF 5F x 65 cm .035 NB PG; Catalog Number: 10732201…

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

Angiodynamics, 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.