State

Maryland product recalls

73,486 recalls have nationwide distribution and so reach Maryland. 8,224 additional recalls listed Maryland specifically in their distribution scope.

What the numbers show

Total: 8,224
Critical: 996
Severe: 2,516
Most recent: 2026-10-14

Of the 8,224 recalls naming Maryland we have scored against our rubric, 996 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,516 (31%) are Severe.

Which agencies issued them

These figures cover only the 8,224 recalls whose distribution notice names Maryland specifically. The 73,486 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22776–22800 of 81710

ModerateFDA (Drugs)·D-0980-2022·2022-06-08
Hand Sanitizer Recall: Storage Temperature Non-Compliance at Family Dollar
Family Dollar Stores is recalling Luxury Hygiene Hand Sanitizer Moisturizing Formula due to cGMP deviations related to improper storage outside labeled temperature requirements.
Product
Luxury Hygiene Hand Sanitizer Moisturizing Formula with Vitamin E, 8 FL. OZ. (236 mL), TSM Brands LLC 540 Equinox Ln Manalapan, NJ 07726, UPC 6 86275 96536 9
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1161-2022·2022-06-08
Universal Nerve Block Tray swab products recalled for manufacturing test validation concerns
Busse Hospital Disposables is recalling Universal Nerve Block Tray units (catalog 9779) due to uncertainty regarding test method validation in manufacturing the included swab/swabstick drug products. No illnesses or injuries have been reported.
Product
Universal Nerve Block Tray Catalog Number: 9779
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1190-2022·2022-06-08
FDA Recalls Swab Products for Manufacturing Validation Uncertainty
Busse Convenience kits containing swab/swabstick products from Professional Disposables International have been recalled by the FDA due to uncertainty about adequate validation of manufacturing test methods.
Product
SS 3.5MM Diamond Tip Trocar - Large Gloves Catalog Number: B1547
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1153-2022·2022-06-08
Swab Drug Products Recalled for Manufacturing Test Method Validation Uncertainty
Busse Convenience kits containing swab/swabstick drug products manufactured by Professional Disposables International (PDI) are being recalled due to uncertainty about the adequacy of test method validation used in manufacturing.
Product
Epidural Tray Catalog 1307
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1185-2022·2022-06-08
Swab and Swabstick Drug Products Recalled Due to Manufacturing Validation Defects
Busse Hospital Disposables is recalling convenience kits containing swab and swabstick drug products due to uncertainty about the adequacy of manufacturing test method validation. Products were distributed nationwide.
Product
4.5MM Pellet Insertion Tray with Large Gloves Catalog Number: B1360
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1179-2022·2022-06-08
Busse swab and swabstick products recalled for validation uncertainty
Busse Convenience kits containing swab and swabstick drug products are recalled nationwide due to uncertainty about whether manufacturing test methods were adequately validated.
Product
3.2MM Pellet Insertion Tray Catalog Number: B1144
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0977-2022·2022-06-08
AMBI Skincare Fade Cream Recalled for Improper Temperature Storage
AMBI Skincare Fade Cream Oily Skin (2 OZ) is recalled nationwide due to improper storage temperature. The product was stored outside the temperature requirements specified on its label.
Product
AMBI Skincare Fade Cream Oily Skin New & Improved, Net Wt. 2 OZ (56g)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1165-2022·2022-06-08
Stereo Breast Biopsy Tray Recalled for Manufacturing Test Validation Uncertainty
Busse Hospital Disposables recalls stereo breast biopsy trays due to uncertainty about the adequacy of manufacturing test validation. The recall affects 23 units distributed nationwide.
Product
Stereo Breast Biopsy Tray Catalog Number: 2383R1
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1148-2022·2022-06-08
Procedure Tray Recalled for Manufacturing Test Method Validation Uncertainty
Busse Hospital Disposables is recalling Procedure Tray Catalog 1065 nationwide due to uncertain validation of manufacturing test methods for the swab/swabstick drug products inside.
Product
Procedure Tray Catalog 1065
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1173-2022·2022-06-08
Pump Refill Kit Recalled Over Uncertain Manufacturing Test Method Validation
Busse Hospital Disposables is recalling Pump Refill Kits nationwide due to uncertainty about whether manufacturing test methods were properly validated. The recall affects 40 units.
Product
Pump Refill Kit Catalog Number: 7347R1
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1189-2022·2022-06-08
Swab Products in Busse Convenience Kits Recalled for Manufacturing Validation Issues
Busse Convenience kits containing swab products are being recalled due to inadequate validation of manufacturing test methods.
Product
SS 4.5MM Pellet Insertion Tray with Medium Gloves Catalog Number: B1365R1
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1200-2022·2022-06-08
Swab and Swabstick Drug Products Recall Due to Manufacturing Test Validation Uncertainty
Busse Convenience kits containing swab and swabstick drug products manufactured by PDI are recalled due to uncertainty about manufacturing test method validation. No illnesses have been reported.
Product
SS 4.5MM Pellet Insertion Tray Catalog Number:B8128R1
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1182-2022·2022-06-08
Busse Convenience Kits Recalled for Manufacturing Test Method Validation Uncertainty
Busse Convenience kits containing swab and swabstick products manufactured by Professional Disposables International are recalled by the FDA due to uncertainty regarding the validation of manufacturing test methods.
Product
SS 3.5Mm Pellet Insertion Tray with large Gloves Catalog Number: B1352R1
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1149-2022·2022-06-08
Cervical Tray Catalog 1089 Recalled for Manufacturing Test Method Validation
Busse Hospital Disposables, Inc. is recalling Cervical Tray Catalog 1089 convenience kits due to uncertainty regarding adequate validation of manufacturing test methods. No illnesses or injuries have been reported.
Product
Cervical Tray Catalog 1089
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0978-2022·2022-06-08
Skincare Product Recalled for Temperature Storage Deviation
Family Dollar Stores is recalling AMBI Skincare Even & Clear Exfoliating Wash because the product was stored outside labeled temperature requirements during manufacturing. No illnesses have been reported.
Product
AMBI Skincare Even & Clear Exfoliating Wash Salicylic Acid Acne Treatment With Oat and Sea Whip, Net Wt. 5 OZ. (141 g)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1163-2022·2022-06-08
Busse Hospital Swab Products Recalled for Manufacturing Validation Uncertainty
Busse Hospital Disposables is recalling Busse Convenience kits containing swab products due to uncertainty about manufacturing test method validation. No illnesses or injuries have been reported.
Product
MBB Tray Catalog Number: 9882
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1177-2022·2022-06-08
Busse Convenience Kits with Swabs Recalled Due to Manufacturing Validation Uncertainty
Busse Convenience kits containing swab/swabstick drug products are recalled due to uncertainty about whether test methods used to validate manufacturing were adequately validated. Distributed nationwide.
Product
Bone Marrow Biopsy Tray Catalog Number: 8917R1
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0979-2022·2022-06-08
Hand Sanitizer Recalled for Improper Temperature Storage Conditions
Family Dollar Stores is recalling Luxury Hygiene Hand Sanitizer due to storage outside of labeled temperature requirements, which may affect product efficacy.
Product
Luxury Hygiene Hand Sanitizer Moisturizing Formula with Vitamin E Advanced Aloe Vera, 8 FL. OZ. (236 mL), TSM Brands LLC 540 Equinox Ln Manalapan, NJ 07726, UPC 6 86275 96537 6
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1194-2022·2022-06-08
Busse Convenience Kits Recalled Due to Inadequate Manufacturing Test Validation
Busse Hospital Disposables is recalling Convenience kits containing swab/swabstick drug products due to uncertainty about the validation of manufacturing test methods. The FDA classified this as a Class II recall.
Product
Female SS 3.5MM Pellet Insertion Tray Catalog Number: B1568
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1183-2022·2022-06-08
Busse Hospital Swab Products Recalled for Manufacturing Validation Uncertainty
Busse Hospital Disposables is recalling swab and swabstick drug products due to uncertainty about whether manufacturing test methods were adequately validated. No illnesses or injuries have been reported.
Product
SS 3.5MM Pellet Insertion Tray with Medium Gloves Catalog Number: B1354
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1162-2022·2022-06-08
Universal Nerve Block Tray Recalled Due to Manufacturing Test Validation Uncertainty
Busse Hospital Disposables recalls Universal Nerve Block Trays and swab products manufactured by PDI due to uncertainty regarding manufacturing test method validation.
Product
Universal Nerve Block Tray Catalog Number: 9818
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1223-2022·2022-06-08
Medtronic NIM Vital Console 4.0 Surgical Nerve Monitoring Device Software Anomaly Recall
Medtronic Xomed is recalling 18 units of the NIM Vital Console 4.0 surgical nerve monitoring device due to an identified software anomaly. Distribution was confirmed in Texas, Colorado, New Jersey, and France.
Product
NIM Vital Console 4.0 (P/N: NIM4CM01) NIM with Software version 1.3.2
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1191-2022·2022-06-08
Busse Convenience Kits Recalled Due to Manufacturing Test Validation Uncertainty
Busse Convenience kits containing swab/swabstick drug products from Professional Disposables International are being recalled due to uncertainty about test method validation during manufacturing. The affected products include lot numbers 2110053 and 2110115, representing 60 units distributed nationwide.
Product
SS 3.5MM Diamond Tip Trocar - Medium Gloves Catalog Number: B1555
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1181-2022·2022-06-08
Medical swab insertion tray recalled due to manufacturing validation uncertainty
Busse Hospital Disposables recalls swab insertion trays due to uncertainty about manufacturing test method validation. The Class II recall affects products nationwide.
Product
SS 3.5Mm Pellet Insertion Tray with large Gloves Catalog Number: B1352
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1224-2022·2022-06-08
Medical Device Patient Interface Recalled Due to Software Anomaly
Medtronic is recalling the NIM Vital Patient Interface 4.0 due to a software anomaly identified in the device. The recall affects 29 units distributed worldwide, including in the US and France.
Product
NIM Vital Patient Interface 4.0 (P/N: NIM4CPB1) NIM with Software version 1.3.2
Category
Medical Device
Distribution
Distributed nationwide