Hazard

Packaging Defect recalls

290 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all packaging defect recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

1–25 of 290

HighFDA (Devices)·Z-2175-2026·2026-05-20
BARD Dynamic Tip Steerable Reprocessed Electrophysiology Catheter Recall
Stryker Sustainability Solutions is recalling BARD Dynamic Tip Steerable reprocessed electrophysiology catheters (Product Number 200131) due to incomplete seals on sterile product packaging. The recall affects 61 units distributed nationwide in the US and in Israel and Canada.
Product
BARD Dynamic Tip Steerable, Product Number 200131; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1990-2026·2026-05-06
DePuy Synthes ATTUNE Revision Hinge Femoral Component Sterility Recall
DePuy Synthes is recalling 3 units of the ATTUNE REVISION HINGE FEMORAL RT SZ 4 CEM due to external sterile packaging found adhered to internal packaging, potentially compromising sterility.
Product
Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 4 CEM. Part Number: 150450204.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1989-2026·2026-05-06
DePuy Synthes ATTUNE Revision Hinge Femoral Component Recall
DePuy Synthes is recalling 3 units of ATTUNE Revision Hinge Femoral RT Size 3 Cement components due to external sterile packaging that was adhered to internal sterile packaging, potentially compromising sterility.
Product
Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 3 CEM. Part Number: 150450203.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1986-2026·2026-05-06
Depuy Synthes ATTUNE Revision Hinge Femoral Component Sterility Compromise
Depuy Synthes is recalling ATTUNE Revision Hinge Femoral components because external sterile packaging was found adhered to internal sterile packaging, potentially compromising sterility.
Product
Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 5 CEM. Part Number: 150450105.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1993-2026·2026-05-06
DePuy Synthes ATTUNE Revision Hinge Femoral implant sterility concern
DePuy Synthes is recalling 3 units of ATTUNE Revision Hinge Femoral RT SZ 8 CEM implants due to external sterile packaging adhered to internal sterile packaging, potentially compromising sterility.
Product
Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 8 CEM. Part Number: 150450208.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1985-2026·2026-05-06
DePuy Synthes ATTUNE Revision Hinge Femoral Component Recall
DePuy Synthes is recalling 3 units of ATTUNE Revision Hinge Femoral Left Size 4 Cement prosthetic components because external sterile packaging was found adhered to internal packaging, potentially compromising sterility.
Product
Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 4 CEM. Part Number: 150450104.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1988-2026·2026-05-06
DePuy Synthes ATTUNE Revision Hinge Femoral Component Sterility Recall
DePuy Synthes is recalling 3 units of ATTUNE REVISION HINGE FEMORAL LT SZ 8 CEM due to external sterile packaging adhered to internal packaging, potentially compromising sterility.
Product
Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 8 CEM. Part Number: 150450108.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1946-2026·2026-05-06
Disposable Mixing Bowls with Spatula recalled for compromised sterile barrier
Zimmer, Inc. is recalling Disposable Mixing Bowls with Spatula (Model 00-5049-011-00) due to package seal defects that may compromise the sterile barrier. Ten complaints have been received identifying incomplete seals, wrinkles, or peeling seals.
Product
Brand Name: Disposable Mixing Bowls with Spatula Product Name: Mixing Bowl and Spatula Model/Catalog Number: 00-5049-011-00 Software Version: N/A Product Description: Mixing Bowl and Spatula Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·26386·2026-04-09
Multiple iron supplement products recalled due to non-child-resistant packaging
Vitaquest International recalls approximately 356,140 iron supplement bottles and packets with non-child-resistant packaging, violating the Poison Prevention Packaging Act. The supplements pose a risk of serious injury or death if swallowed by young children.
Product
Various Brands of Iron-Containing Dietary Supplements
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1328-2026·2026-02-18
Medline pediatric catheter securement kits recalled for potential open packaging seals
Medline Industries is recalling 450 pediatric catheter securement dressing kits nationwide due to potential open seals on BD ChloraPrep applicator packaging. Open seals may compromise product sterility and integrity.
Product
Medline medical convenience kits packaged as: PEDIATRIC CATH SECUREMENT DRSG, Kit SKU DYNDC3108
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1334-2026·2026-02-18
Medline Medical Kits With BD ChloraPrep Swabsticks Recalled for Open Packaging Seals
Medline Industries is recalling 8,445 medical convenience kits nationwide due to open seals on BD ChloraPrep Triple Swabstick applicator packaging. The defect may compromise product sterility.
Product
Medline medical convenience kits packaged as: ) LVAD DRESSING CHANGE TRAY, Kit SKU DM320C; 2) PORT AND IO ACCESS DRESSING KI, Kit SKU DT15780A; 3) PORT-A-CATH DRESSING CHANGE TR, Kit SKU DT16615; 4) LARGE BORE CENTRAL LINE DRSG C, Kit SKU DT19660; 5) CENTRAL LINE DRESS
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1172-2026·2026-02-04
AlternatiV+ Max Knotless Anchor Recalled for Device Failure Reports
The FDA has recalled 2,569 units of the AlternatiV+ Max Knotless Anchor due to reports of device failures including anchor breakage, bending, and pull-out. The devices were distributed nationwide.
Product
AlternatiV+ Max Knotless Anchor
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0922-2026·2025-12-24
Medline Sterile Kelly Forceps Recalled Due to Weak Packaging Seals
Medline is recalling sterile Kelly forceps (Item DYNJ04048) distributed in CA, CO, IL, KS, and MI. Weak packaging seals may compromise sterility, increasing the risk of infection if the product is used.
Product
FORCEP, STD STR, STERILE KELLY, 5.5 IN, Item Number DYNJ04048
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0927-2026·2025-12-24
Halyard EP LAB Pack recalled for incomplete header bag seal
AVID Medical is recalling 240 units of Halyard EP LAB Pack (Catalog ESJH009-03) due to potential incomplete seals on header bags. The affected lot was distributed to facilities in Georgia, Illinois, Nebraska, and Maryland.
Product
Halyard, EP LAB PK. Catalog Number: ESJH009-03.
Category
Medical Device
Distribution
4 states
HighFDA (Devices)·Z-0898-2026·2025-12-17
CURAD Germ-Shield Fabric Bandages recalled for potentially compromised sterility
Medline is recalling CURAD Germ-Shield Touch-Free Fabric Bandages because packaging seals may be open, potentially compromising product sterility. Consumers should stop using affected units.
Product
CURAD Germ-Shield Touch-Free Fabric Bandages, Sterile, 0.75" x 3", 30/Box, Medline Item Number CUR1930F
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0901-2026·2025-12-17
Medline Quick Strip Sterile Adhesive Bandages recalled for compromised packaging seals
Medline is recalling all lots of Quick Strip Plastic Sterile Adhesive Bandages (1" x 3") due to open seals in packaging that may compromise sterility. No injuries have been reported.
Product
Quick Strip Plastic Sterile Adhesive Bandages, 1" x 3", Medline Item Number NON25600QS
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0423-2026·2025-11-12
Triple Lumen Catheter Trays Recalled for Packaging Seal Integrity Issues
Mozarc Medical is recalling 3,258 MAHURKAR triple lumen catheter trays due to potential seal integrity issues with the header bag packaging. The affected units were distributed nationwide.
Product
MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions with IC Components: 12 Fr/Ch (4.0 mm) x 20 cm;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0148-2026·2025-10-22
BioPro Femoral Head recalled due to packaging sterility compromise risk
BioPro, Inc. is recalling BioPro Femoral Head prosthetics due to a potential packaging defect that could compromise sterility. The defect may result in infection risk if the device is implanted.
Product
BioPro Femoral Head (Metal 22, 28, 32, 36, 40) cobalt chromium and ceramic heads Part ID/Description: 18593 HEAD FEMORAL 22MM -3 18594 HEAD FEMORAL 22MM +0 19003 HEAD FEMORAL 28MM-6 19004 HEAD FEMORAL 28MM-3 19005 HEAD FEMORAL 28MM+0 19006 HEAD FEMORAL 28MM+3 19007 HEAD
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0149-2026·2025-10-22
BioPro Endo Head orthopedic implants recalled for sterile barrier packaging defect
BioPro Endo Head orthopedic implants (147 units distributed to Texas and Michigan) are recalled due to a packaging defect that may compromise sterility, presenting a potential infection risk if implanted.
Product
BioPro Endo Head (Metal uni-polar, 38-55) Product Number/Description 10179 ENDO MD 38 10180 ENDO MD 41 10181 ENDO MD 43 10182 ENDO MD 45 10183 ENDO MD 47 10184 ENDO MD 49 10185 ENDO MD 51 10186 ENDO MD 53 10187 ENDO MD 55 10188 ENDO SH 38 10189 ENDO SH 41 10190 E
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0152-2026·2025-10-22
BioPro Endo Head Ceramic Implants Recalled for Sterility Compromise
BioPro is recalling 147 ceramic endo head implants due to a potential packaging defect that could compromise sterility. If implanted with compromised sterility, the device could pose an infection risk.
Product
BioPro Endo Head (Ceramic) Product ID/Description 13006 ENDO MODULAR CERAMIC SH 38 13012 ENDO MODULAR CERAMIC SH 51 13013 ENDO MODULAR CERAMIC MD 38 13019 ENDO MODULAR CERAMIC MD 51 13007 ENDO MODULAR CERAMIC SH 41 13008 ENDO MODULAR CERAMIC SH 43 13009 ENDO MODULAR CER
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0151-2026·2025-10-22
BioPro Ceramic Femoral Head Implants Recalled for Potential Sterility Breach
BioPro is recalling 147 ceramic femoral head implants due to a packaging defect that could compromise the sterile barrier. The defect poses a potential infection risk if the implanted device becomes contaminated.
Product
BioPro Femoral Head (Ceramic heads 28-30) Product ID/Description 19023 HEAD FEMORAL CERAMIC 28MM -3 19024 HEAD FEMORAL CERAMIC 28MM +0 19025 HEAD FEMORAL CERAMIC 32MM -3 19026 HEAD FEMORAL CERAMIC 32MM +0 19027 HEAD FEMORAL CERAMIC 32MM +3
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2510-2025·2025-09-10
Wound dressing recall due to potential sterile barrier packaging failures
Integra's MediHoney Hydrogel Adhesive Sheet dressings may have packaging failures compromising sterility. Affected units are being recalled worldwide.
Product
Brand Name: MediHoney¿ Product Name: MediHoney¿ Hydrogel Adhesive Sheet Model/Catalog Number: 31722, 31744 Product Description: MEDIHONEY¿ HCS ADHESIVE SHEET DRESSING with LEPTOSPERMUM HONEY is a moist wound dressing made of Leptospermum Honey (+15) in combination with a hydro
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2505-2025·2025-09-10
Medical wound dressing recalled for sterile packaging barrier failures
Integra LifeSciences is recalling MediHoney Paste, a medical wound dressing, due to packaging failures that could compromise the sterile barrier. The recall affects 15,441 units distributed worldwide.
Product
Brand Name: MediHoney ¿ Product Name: MediHoney¿ Paste Model/Catalog Number: 31505 Product Description: MediHoney¿ Paste with Active Leptospermum Honey is a moist dressing made of 100% Active Leptospermum medical grade Honey. The dressing helps maintain a moist environment con
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0616-2025·2025-09-10
Chlorpromazine Hydrochloride Tablets Recalled for Contaminated Packaging
Amneal Pharmaceuticals recalls specific lots of Chlorpromazine Hydrochloride 25 mg tablets due to a micro-organism detected in packaging material. The medication itself remains uncontaminated.
Product
CHLORPROMAZINE HYDROCHLORIDE — CHLORPROMAZINE HYDROCHLORIDE (CHLORPROMAZINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2109-2025·2025-07-16
Alcon Constellation Vision System Procedure Packs Recalled for Sterility Risk
Alcon Laboratories is recalling certain Constellation Vision System Combined Procedure Paks (89,495 units) due to potential damage to the lidding that may compromise sterility. Affected products were distributed worldwide.
Product
Brand Name: Alcon Laboratories, Inc. Product Name: Constellation Vision System Combined Procedure Pak Model/Catalog Number: Many - See 'Attachment 1 - Affected Product List' Software Version: N/A Product Description: Surgical procedure pack to interface with Alcon Constellati
Category
Medical Device
Distribution
Distributed nationwide