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 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)

Medical devices

Reported Aug 14, 2019

Alinity i Ferritin Reagent Kit, List Number 07P6530 The Alinity i Ferritin assay is a chemiluminescent microparticle…

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

Abbott Ireland Diagnostics Division

FDA (openFDA device enforcement)

Medical devices

Reported Aug 14, 2019

STERILE GRAVES VAGINAL SPECULUM MEDIUM Kit Code # GVS10MST - Product Usage:The speculum is used to spread the walls of…

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

Centurion Medical Products Corporation

12 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 14, 2019

IDEAL IMPLANT Structured Breast Implant, saline breast implant, in the following sizes: 210cc, 240cc, 270cc, 300cc,…

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

Ideal Implant Incorporated

FDA (openFDA device enforcement)

Medical devices

Reported Aug 14, 2019

SmartRelease Endoscopic Carpal Tunnel Release Handpiece (ECTR handpiece), part numbers 81014 and 83014

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

MicroAire Surgical Instruments, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 14, 2019

Human Assayed Multi-Sera Level 2, Model NO. HN1530 Product Usage: This product is intended for in vitro diagnostic use,…

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

Randox Laboratories, Limited

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 14, 2019

Dimension¿ Ferritin (FERR) Flex¿ reagent cartridge DM FERR Product Usage: The FERR Flex reagent cartridge is intended…

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 14, 2019

Shirakiku FISH CAKE IWASHI TEN SK F 20/150 g; Net WT. 5.29 oz. Keep frozen, 7 pcs. UPC 074410925246 Distributed by…

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

Wismettac Asian Foods, Inc.

7 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Aug 7, 2019

Bento Express Fully Cooked Pink Salmon in a Teriyaki Sauce with Snow Peas, Garnished with Sesame Seeds. Served on…

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

Bento Sushi

FDA (openFDA food enforcement)

Food

Reported Aug 7, 2019

Dolfin Dark Chocolate with Pink Peppercorns Net Wt 2.47 oz (70g), UPC 5 413415 233300, bar code 1938090025

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

Dolfin S.A.

FDA (openFDA food enforcement)

Food

Reported Aug 7, 2019

Green Giant Fresh Cauliflower Sweet Potato Crumbles; Chopped Sweet Potato and Cauliflower 1 lb.(16 oz.) (454 g) plastic…

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

Growers Express S

12 more products in this recall

FDA (openFDA food enforcement)

Medical devices

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)

Medical devices

Reported Jul 31, 2019

ARCHITECT BNP Calibrators Ptoduct Usage: The ARCHITECT BNP Calibrators are for the calibration of the ARCHITECT iSystem…

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

Abbott Laboratories

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 31, 2019

Lisy Ground Cinnamon Canela Molida NET WT./CONT. NETO 13 OZ (368g) and 2 OZ (57g)

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

EL Chilar Huff

FDA (openFDA food enforcement)

Food

Reported Jul 31, 2019

DaVinci Laboratories of Vermont Omega 3-1,000 in a white bottle labeled as Dim Plex, 60 count UPC Code 026664273161

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

FoodScience Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Jul 31, 2019

PulsioFlex Monitoring System, Part Number: 6882747, Model Number: PC400 3 R0. Usage: The PulsioFlex Monitoring System…

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

Getinge US Sales LLC

FDA (openFDA device enforcement)

Meat & poultry

Reported Jul 31, 2019

Conagra Brands, Inc. Recalls Canned Beef Products Due to Possible Processing Defect

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

Hometown Food Company

USDA FSIS

Food

Reported Jul 31, 2019

Jelly Belly Licorice Bridge Mix. Net Wt. 9 oz. (85g); 12 individual 3 oz. bags per caddy UPC: 071567981675 Manufactured…

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

Jelly Belly

FDA (openFDA food enforcement)

Medical devices

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)

Medical devices

Reported Jul 31, 2019

Merge PACS versions 7.3, 7.3.1, 8.0 and 8.0.1

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

Merge Healthcare, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 31, 2019

RX Daytona, Model Nos. RX4040 and RX4041

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

Randox Laboratories, Limited

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 31, 2019

Wegmans Mini Ultimate Carrot Cake (Carrot Cake with Cream Cheese Frosting), 17oz, Sold in clear plastic cake clam…

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

Wegmans Food Markets, Inc.

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 31, 2019

GammaPod Stereotactic Radiotherapy System Model A, REF XMSGP030A00-0.02 Product Usage: GammaPod is a teletherapy device…

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

Xcision Medical Systems, LLC

FDA (openFDA device enforcement)

Meat & poultry

Reported Jul 25, 2019

Home Market Foods, Inc. Recalls Frozen Ready-To-Eat Beef and Pork Meatball Products due to Misbranding and Undeclared…

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

Home Market Foods, Inc.

USDA FSIS

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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.