State

Guam product recalls

72,907 recalls have nationwide distribution and so reach Guam. 385 additional recalls listed Guam specifically in their distribution scope.

What the numbers show

Total: 385
Critical: 14
Severe: 37
Most recent: 2026-01-28

Of the 385 recalls naming Guam we have scored against our rubric, 14 (4%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 37 (10%) are Severe.

Which agencies issued them

These figures cover only the 385 recalls whose distribution notice names Guam specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1376–1400 of 73292

SevereFDA (Devices)·Z-2254-2026·2026-06-10
BD Whitacre 25 gauge spinal trays recalled over bupivacaine quality issues
BD Spinal Trays with a Whitacre 25 G needle, catalog number 405658, are being recalled as a sub-recall of the Huons bupivacaine product recall. 150 units affected.
Product
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 2 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405658.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2249-2026·2026-06-10
BD Quincke 25G spinal trays recalled in Huons bupivacaine sub-recall
BD Spinal Trays with Quincke needle 25 G, which contain bupivacaine with dextrose, are being recalled as a sub-recall of the Huons bupivacaine product recall. 3,130 units are affected.
Product
BD¿Spinal Tray with BD¿Quincke Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 405621, 405735.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2278-2026·2026-06-10
Design Options spinal trays recalled over Huons bupivacaine quality issues
Design Options spinal needle anesthesia procedure kits are being recalled because they contain Bupivacaine Hydrochloride in Dextrose Injection subject to the Huons recall.
Product
Design Options Spinal Tray Spinal Needle Anesthesia procedure kits: Material Description (Material Number): SSK H M C 20061890 (560074), SSK S C H (560214), SSK BJC H S (ORIGINAL CUST) (560272), SSK CA P M C (ORIGINAL CUST) (560327), SSK T M H (560394), SSK S O 20070208 (
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2223-2026·2026-06-10
Ivenix pump software may report false battery health and shut down
The Ivenix Infusion System Large Volume Pump software is being recalled because a software anomaly can report a false battery-health value and trigger a shutdown alarm.
Product
LVP software of the Ivenix Infusion System (IIS); Product Code LVP-SW-0005.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2250-2026·2026-06-10
BD Quincke 26G spinal trays recalled in Huons bupivacaine sub-recall
BD Spinal Trays with Quincke needle 26 G, which contain bupivacaine with dextrose, are being recalled as a sub-recall of the Huons bupivacaine product recall. 890 units are affected.
Product
BD¿Spinal Tray with BD¿Quincke Needle 26 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405632.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2253-2026·2026-06-10
BD combined Whitacre and Quincke spinal trays recalled over bupivacaine
BD Spinal Trays containing both a Whitacre 25 G and a Quincke 22 G needle are being recalled as a sub-recall of the Huons bupivacaine product recall. 290 units affected.
Product
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in., BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405741.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2256-2026·2026-06-10
BD spinal trays recalled as a sub-recall of Huons bupivacaine
BD Spinal Trays with Whitacre needle, which contain bupivacaine with dextrose, are being recalled as a sub-recall of the Huons bupivacaine product recall.
Product
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405671.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0565-2026·2026-06-10
CareOne extra strength calcium antacid tablets contain metallic particles
CareOne Extra Strength Calcium Antacid, calcium carbonate 750 mg, is being recalled because of the presence of small metallic particles in the chewable tablets.
Product
EXTRA STRENGTH ANTACID — EXTRA STRENGTH ANTACID (CALCIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2287-2026·2026-06-10
Philips Azurion 5M20 Roadmap Pro may produce unusable dark images
Philips Azurion 5M20 systems with the Roadmap Pro software key are being recalled because a pedal tap may cause a dark, clinically unusable image on the next fluoroscopy run.
Product
Philips Azurion 5M20, Model Numbers: 722228 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V381000·2026-06-10
Denago EV Recalls Multiple Models for Missing Pedestrian Warning Sounds
Denago EV is recalling 2024-2026 electric vehicles that may fail to emit pedestrian warning sounds, increasing the risk of crashes.
Product
DENAGO EV — DENAGO EV NOMAD XL, ROVER XL, ROVER XL6, ROVER XXL
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·H-1015-2026·2026-06-10
Imitation Cajun crab seafood salad does not declare crab and pollock
Albertsons store-made Seafood Salad Imitation Cajun Crab is being recalled because the contains statement does not declare crab and pollock. 53 units are affected.
Product
UPC 23114800000 SEAFOOD SALAD IMITATION CAJUN CRAB This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0558-2026·2026-06-10
Tums assorted fruit antacid tablets contain small metallic particles
Tums Antacid Assorted Fruit tablets, calcium carbonate 1000 mg in 160-count bottles, are being recalled because of small metallic particles in the chewable tablets.
Product
HALEON CALCIUM CARBONATE TUMS ANTACID, Assorted Fruit Tablets, 1000 mg, 160-count bottle, Haleon, Warren, NJ 07059, UPC 3 07660 74610 2.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-1036-2026·2026-06-10
Albertsons sesame mandarin salads do not declare almond allergen
Albertsons store-made sesame and mandarin salads are being recalled because the contains statement does not declare almond. 196 units are affected.
Product
UPC 21870200000 KITCHEN SALAD SESAME ASIAN LARGE SS COLD UPC 27817500000 Ready Meals SALAD MANDARIN SESAME NOODLE SS UPC 29326100000 SALAD SESAME MANDARIN FS COLD This is Albertson's store-made item and sold by unit or random weight at point of s
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0574-2026·2026-06-10
GoodSense antacid chewable tablets contain small metallic particles
GoodSense Extra Strength Antacid Tablets, calcium carbonate 750 mg, are being recalled because of the presence of a foreign substance: small metallic particles in the chewable tablets.
Product
GOODSENSE EXTRA STRENGTH ANTACID — GOODSENSE EXTRA STRENGTH ANTACID (CALCIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2303-2026·2026-06-10
BD Pyxis MedBank Tower fingerprint scanner may overheat and burn
The BD Pyxis MedBank Tower medication cabinet is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.
Product
BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0564-2026·2026-06-10
Market Basket ultra strength antacid tablets contain small metallic particles
Market Basket Antacid, calcium carbonate 1000 mg ultra strength, is being recalled because of the presence of small metallic particles in the chewable tablets.
Product
MARKET BASKET ANTACID Calcium Carbonate 1000 mg, ULTRA STRENGTH, 72 Tablets, Distributed by: De Moules Supermarkets, Inc.,Tewksbury, Mass 01875, UPC 0 49705 83149 6.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2302-2026·2026-06-10
BD Pyxis MedStation fingerprint scanners may overheat and cause burns
BD Pyxis MedStation ES Tower medication cabinets are being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.
Product
BD Pyxis MedStation ES Tower REF: 352 Medication cabinet
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0578-2026·2026-06-10
TopCare extra strength antacid tablets contain small metallic particles
TopCare Health Extra Strength Antacid Tablets, calcium carbonate 750 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.
Product
TOPCARE EXTRA STRENGTH ANTACID — TOPCARE EXTRA STRENGTH ANTACID (CALCIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0977-2026·2026-06-10
Albertsons Italian super sub sandwich does not declare pistachio
Albertsons store-made Kitchen Sandwich Italian Super Sub is being recalled because the contains statement does not declare pistachio. 28 units are affected.
Product
UPC 21243500000 KITCHEN SANDWICH ITALIAN SUPER SUB SS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2289-2026·2026-06-10
Philips Azurion 7B20/15 systems may show unusable dark fluoroscopy images
Philips Azurion 7B20/15 systems with the Roadmap Pro software key are being recalled because a pedal tap may produce a dark image that is not clinically usable. 156 units affected.
Product
Philips Azurion 7B20/15, Model Numbers: 722068, 722226 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-1025-2026·2026-06-10
Pad Thai chicken with pot stickers does not declare anchovy
Albertsons store-made Ready Meals Wok Pad Thai Chicken with Pot Stickers is being recalled because the contains statement does not declare anchovy. 39 units are affected.
Product
UPC 21380100000 Ready Meals WOK PAD THAI CHICKEN WITH POT STICKERS SS This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-0980-2026·2026-06-10
Albertsons banana nut muffins do not declare walnut allergen
Albertsons store-made Banana Nut Muffins in 2 count and 4 count packs are being recalled because the contains statement does not declare walnut. 434 units are affected.
Product
UPC 22454900000 MUFFINS BANANA NUT 2CT UPC 22120200000 MUFFINS BANANA NUT 4CT This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0573-2026·2026-06-10
H-E-B extra strength antacid tablets contain small metallic particles
H.E.B Extra Strength Calcium Carbonate Antacid Tablets, 750 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.
Product
HEB EXTRA STREGTH ANTACID — HEB EXTRA STREGTH ANTACID (CALCIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0991-2026·2026-06-10
Albertsons 16-inch Italian sampler tray does not declare almond
An Albertsons store-made 16-inch Italian sampler tray is being recalled because the contains statement does not declare almond. Nine units are affected.
Product
UPC 29153000000 SAMPLER TRAY ITALIAN 16 INCH This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2275-2026·2026-06-10
PhaseOne antimicrobial solution sprayer springs may corrode into the product
PhaseOne Antimicrobial Solution is being recalled because the stainless steel spring inside the sprayer can corrode, releasing trace metallic elements into the solution.
Product
PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050
Category
Medical Device
Distribution
Distributed nationwide