State

New Hampshire product recalls

73,388 recalls have nationwide distribution and so reach New Hampshire. 4,472 additional recalls listed New Hampshire specifically in their distribution scope.

What the numbers show

Total: 4,472
Critical: 606
Severe: 1,042
Most recent: 2026-09-23

Of the 4,472 recalls naming New Hampshire we have scored against our rubric, 606 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,042 (23%) are Severe.

Which agencies issued them

These figures cover only the 4,472 recalls whose distribution notice names New Hampshire specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

21276–21300 of 77860

HighFDA (Drugs)·D-0958-2022·2022-06-08
Injectable Hydromorphone Recalled for Lack of Sterility Assurance
Nephron Sterile Compounding Center is recalling Hydromorphone HCl Injection due to lack of assurance of sterility. The recall affects 6,210 pre-filled syringes distributed nationwide.
Product
Hydromorphone HCl Injection, USP, 6 mg/30 mL (0.2 mg/mL), 30 mL Pre-Filled Syringe, 5 x 30 mL Pre-Filled Syringes, 6 x 5 Syringe Carton, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-529-30
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0963-2022·2022-06-08
Neostigmine Methylsulfate Injection Recalled Due to Sterility Assurance Failure
Nephron Sterile Compounding Center is recalling Neostigmine Methylsulfate Injection due to lack of assurance of sterility. The compounded injectable drug may not meet sterile product standards.
Product
Neostigmine Methylsulfate Injection, USP, 5 mg/5 mL (1 mg/mL), Preservative Free, 5 mL Pre-Filled Syringe, 5 x 5 mL Pre-Filled Syringes, 6 x 5 Syringe Carton, Rx Only Nephron 503B outsourcing facility 4500 12th St. Extension West Columbia, SC 29172 NDC: 69374-902-05
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0976-2022·2022-06-08
AMBI Skincare Fade Cream Recalled for Temperature Storage Deviations
AMBI Skincare Fade Cream is being recalled nationwide due to cGMP violations. The product was stored outside its labeled temperature requirements during manufacturing.
Product
AMBI Skincare Fade Cream Normal Skin, Net Wt. 2 OZ. (56g)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1147-2022·2022-06-08
I.V. Start Kit with Swab Products Recalled for Manufacturing Validation Issues
Busse Hospital Disposables is recalling I.V. Start Kits containing swab products due to inadequate validation of manufacturing test methods. Approximately 2,475 units nationwide may be affected.
Product
I.V. Start Kit - Tegaderm Dressing - Catheter Securement - Prevantics Catalog Number: 822
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1213-2022·2022-06-08
Abbott FIRMap Catheter Recalled for Incorrect Product Labeling
Abbott is recalling 40 units of FIRMap® Catheter, 60mm Basket due to incorrect product labeling. The recall affects devices distributed in Missouri, California, Ohio, Washington and internationally in Italy and Netherlands.
Product
FIRMap" Catheter, 60mm Basket
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1180-2022·2022-06-08
Swab and Swabstick Drug Products Recalled Due to Validation Uncertainty
Busse Convenience kits with swab and swabstick drug products are being recalled because the validation of the test methods used during manufacturing is uncertain.
Product
"3.2MM Pellet Insertion Tray with Medium Gloves" Catalog Number: B1351
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1142-2022·2022-06-08
Locking Cap for PD Catheter Adapter Distributed Without FDA Clearance
Baxter Healthcare is recalling locking caps for peritoneal dialysis catheters that were distributed without FDA regulatory clearance. These devices were released into the U.S. market in error.
Product
Locking Cap for PD Catheter Adapter
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1193-2022·2022-06-08
Busse Convenience Kit Swab Products Recalled for Test Method Validation Issues
Busse Convenience kits containing swab and swabstick drug products manufactured by Professional Disposables International are being recalled due to uncertainty about test method validation during manufacturing.
Product
SS 4.5MM DIAMOND TIP TROCAR WITH MEDIUM GLOVES Catalog Number: B1560
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1195-2022·2022-06-08
Convenience Kits with Drug Swab Products Recalled for Validation Uncertainty
Busse Convenience kits containing swab/swabstick drug products are being recalled nationwide due to uncertainty about the adequacy of the validation of manufacturing test methods.
Product
Male SS 4.5MM Pellet Insertion Tray Catalog Number: B1570
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1184-2022·2022-06-08
Pellet Insertion Tray Recall for Uncertain Manufacturing Test Validation
Busse Hospital Disposables is recalling SS 3.5MM Pellet Insertion Tray kits nationwide. The kits contain swab products with uncertain manufacturing test method validation.
Product
SS 3.5MM Pellet Insertion Tray with Medium Gloves Catalog Number: B1354R1
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1144-2022·2022-06-08
Baxter Effluent Sample Bags Recalled for Lack of FDA Clearance
Baxter Healthcare recalled 78 Effluent Sample Bags that were distributed without FDA regulatory clearance. The product was distributed in error across eight states.
Product
Effluent Sample Bag
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1214-2022·2022-06-08
BD Anti-Kappa Flow Cytometry Reagents Recalled for Uncharacteristic Flow Profiles
BD Anti-Kappa APC and PE reagents used in flow cytometry testing may exhibit uncharacteristic flow profiles, potentially affecting test accuracy. Worldwide distribution to 249 units across US states and Taiwan.
Product
BD Anti-Kappa APC (Cat. No. 341098) is an analyte specific reagent for the Anti-Kappa antibody, which specifically recognizes the kappa light chains of human immunoglobulins. Anti-Kappa is used for in vitro identification of cells expressing the kappa light chains using flow…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1156-2022·2022-06-08
Medical Swabs Recalled Due to Manufacturing Test Method Validation Uncertainty
Busse Convenience kits containing medical swabs and sticks have been recalled due to uncertainty about whether the manufacturing test methods used were adequately validated.
Product
Port Tray Catalog 7607
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1192-2022·2022-06-08
Busse Hospital Disposables Convenience Kit Swab Recall for Test Validation Uncertainty
Busse Hospital Disposables is recalling convenience kits containing swab products due to uncertainty about adequate validation of manufacturing test methods.
Product
SS 4.5MM DIAMOND TIP TROCAR WITH LARGE GLOVES Catalog Number:B1559
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0981-2022·2022-06-08
Aveeno Daily Moisturizing Lotion recalled due to improper storage conditions
Family Dollar and Johnson & Johnson Consumer are recalling Aveeno Daily Moisturizing Lotion due to cGMP violations involving improper storage temperature. No illnesses have been reported.
Product
Aveeno Daily Moisturizing lotion Fragrance Free with Soothing Oat & Rich Emollients, Net Wt. 5 oz (141 g), Distributed by Johnson & Johnson Consumer, Inc. Skillman, NJ 08558, UPC 3 81137-001530 7
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1178-2022·2022-06-08
Procedural Accessory Kit Recalled for Manufacturing Validation Uncertainty
Busse Hospital Disposables is recalling Procedural Accessory Kits containing swabs due to uncertainty regarding the validation of manufacturing test methods. No illnesses or injuries have been reported.
Product
Procedural Accessory Kit Catalog Number: 9665R2
Category
Medical Device
Distribution
Distributed nationwide
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