infant product Recalls

794 recalls tagged with “infant product”.

Food & Beverages
HIGH
FDA FOOD

Wholesale Produce Supply LLC Cantaloupe Chunks Recall Expands for Listeria Contamination

Wholesale Produce Supply LLC recalled 307 cases of cantaloupe chunks sold under Fresh & Finest, Harvest Cuts and other labels. The recall targets a broad range of container sizes and UPCs in IA, IL, ND, NE and WI. The recall cites potential Listeria monocytogenes contamination and is classified as Class I.

Wholesale Produce Supply LLC
Potential Listeria
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Health & Personal Care
HIGH
FDA DEVICE

Synthes 5.0mm IM Nail Screw Recalled for Labeling Error (2025)

Synthes USA recalled 122 locking intramedullary nail screws used in RFN-Advanced and Tibial Nail Advanced systems. The recall covers worldwide distribution including the US and Canada. The packaging labeling misstates screw length while the etched length on the screw is correct. Healthcare providers should stop using the device immediately and follow recall instructions from Synthes.

Synthes
Although the
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Food & Beverages
HIGH
FDA FOOD

Albertsons Store-Made Grilled Chicken & Basil Pasta Extra Large Recalled for Listeria (2025)

Albertsons Companies is recalling store-made Grilled Chicken & Basil Pasta Extra Large sold under Carrs-Safeway, Eagle and Safeway banners. The product contains a bowtie pasta ingredient recalled for Listeria monocytogenes contamination. It was distributed in AK, AR, AZ, CA, CO, HI, LA, NE, NM, NV, OK, SD, TX, UT and WY. Stop using the product and contact Albertsons for refund or replacement.

Albertsons
Listeria monocytogenes.
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Food & Beverages
HIGH
FDA FOOD

Wholesale Produce Supply LLC Recalls 307 Cases of Cut Fresh Fruit Mix Over Listeria Risk (2025)

Wholesale Produce Supply LLC recalls 307 cases of Cut Fresh Fruit Mix due to potential Listeria monocytogenes contamination. The product was packed by WPS in Minneapolis, MN and distributed to five Midwest states. Consumers should not eat the recalled fruit and should contact the distributor for refund or replacement.

Wholesale Produce Supply LLC
Potential Listeria
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Food & Beverages
HIGH
FDA FOOD

Wegmans Recalls 521 Large Ultimate Strawberry Topped Cheesecake Over Undeclared Pecans (2025)

Wegmans Food Markets recalled 521 units of Wegmans Large Ultimate Strawberry Topped Cheesecake distributed in Virginia, Maryland, North Carolina and Washington, D.C. The cake contains undeclared pecans, posing an allergen risk. Consumers should not eat the product and should contact Wegmans for a refund or replacement.

Wegmans Food Markets
Contains undeclared
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Food & Beverages
HIGH
FDA FOOD

Wholesale Produce Recall: Cut Fresh Melon Mix Recalled Over Listeria Contamination Risk (2025)

Wholesale Produce Supply LLC DBA recalled 307 cases of Cut Fresh Melon Mix due to potential Listeria monocytogenes contamination. The recall covers multiple Melon Mix products packed by WPS in Minneapolis and distributed to IA, IL, ND, NE, and WI. Consumers should not eat the product and should seek refunds or replacements.

WHOLESALE PRODUCE SUPPLY LLC
Potential Listeria
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Health & Personal Care
HIGH
FDA DEVICE

Synthes 5.0mm IM Nail Locking Screws Recalled for Packaging Length Label Error (120 Units, 2025)

Synthes (USA) Products LLC recalled 120 low-profile locking screws for intramedullary nails used in the RFN-Advanced Retrograde Femoral Nailing System and the Tibial Nail Advanced System. The recall covers devices distributed worldwide through healthcare providers. The external packaging mislabels screw lengths: 42 mm screws are labeled 46 mm and 46 mm screws are labeled 42 mm. Hospitals and spine

Synthes
Although the
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Food & Beverages
HIGH
FDA FOOD

Albertsons Store-Made Ready Meals Smoked Mozzarella Penne Pasta Salad Recalled for Listeria monocyt—

Albertsons Companies is recalling Ready Meals Smoked Mozzarella Penne Pasta Salad sold under Carrs-Safeway, Eagle and Safeway banners in Alaska and 14 other states after the FDA linked the product to Listeria monocytogenes. The in-store Penne pasta ingredient recall prompted the action. Consumers should not eat the product and should contact Albertsons Companies LLC for refund or replacement.

Albertsons Companies
Listeria monocytogenes.
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Food & Beverages
HIGH
FDA FOOD

Wholesale Produce Supply LLC Cut Fresh Fruit Tray Recalled for Listeria Risk (2025)

Wholesale Produce Supply LLC recalls 307 cases of Cut Fresh Fruit Tray with Strawberries after potential Listeria monocytogenes contamination. The recall covers trays packed in Minneapolis, MN and distributed to Iowa, Illinois, North Dakota, Nebraska and Wisconsin. The product should not be consumed and refunds or replacements are being offered. The recall is active as of the latest notice.

Wholesale Produce Supply LLC
Potential Listeria
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Food & Beverages
HIGH
FDA FOOD

Albertsons Basil Pesto Bow Tie Pasta Salad Recalled for Listeria (2025)

Albertsons Companies recalled store-made Basil Pesto Bow Tie Pasta Salad sold under banners including Albertsons, Pavilions, Randalls, Safeway, Tom Thumb, and Vons after Listeria monocytogenes contamination. The bowtie pasta ingredient used in the deli item was recalled for this reason. Consumers who purchased the product should not consume it and should contact Albertsons Companies for refund or

Albertsons Companies
Listeria monocytogenes.
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Food & Beverages
HIGH
FDA FOOD

Albertsons Recalls Store-Made Ready Meals Pesto Bowtie Pasta Salad Over Listeria (2025)

Albertsons recalled store-made Ready Meals Pesto Bowtie Pasta Salad sold at banners including Albertsons, Pavilions, Randalls, Safeway, Tom Thumb and Vons. The recall concerns a bowtie pasta ingredient contaminated with Listeria monocytogenes. Do not consume the product and seek a refund or replacement from Albertsons Companies LLC.

Albertsons
Listeria monocytogenes.
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Food & Beverages
HIGH
FDA FOOD

Reser’s Fine Foods Salad Kits Recalled Over Listeria Risk in 795 Cases Distributed Across 9 States

A high-risk recall affects 795 cases of Reser’s Fine Foods Basil Pesto Bowtie Pasta Kit distributed in Arizona, California, Colorado, Utah and Washington. The recall covers item #404736 with use-by dates in October 2025. Consumers should not consume these salad kits and should contact Reser’s for refunds or replacements.

Reser's Fine Foods
Salad Kits
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Food & Beverages
HIGH
FDA FOOD

Reser’s Fine Foods Salad Kit Recalled for Listeria Contamination (2025)

Reser’s Fine Foods recalled 3,252 cases of Basil Pesto Bowtie Pasta Kit Item V, UPC 13454 38053, distributed in AZ, CA, CO and TX. The recall concerns potential contamination with Listeria monocytogenes. Consumers should not eat the product and should seek refund or replacement.

Reser’s Fine Foods
Salad Kits
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Recalled RELIEVE Numbing Cream – Outer Packaging
HIGH
CPSC

Mad Rabbit RELIEVE Lidocaine Numbing Cream Recalled for Non‑Child-Resistant Packaging

Mad Rabbit recalls RELIEVE lidocaine numbing cream due to non‑compliant packaging that could allow poisoning of young children. The recall covers a product sold under the Mad Rabbit brand and issued on 2025-09-25. The packaging does not meet the Poison Prevention Packaging Act requirement for child resistance. Consumers should stop using the product immediately and contact Mad Rabbit for a free, a

Mad Rabbit
The numbing
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Recalled Persilux Zebra Blinds
HIGH
CPSC

Persilux Zebra Blinds Recalled for Strangulation Risk, Sold on Amazon

Persilux recalled zebra blinds sold on Amazon after safety hazards were found. The recall cites long operating cords that can cause strangulation and entanglement. The company offers a free repair kit and instructions to remove cords. Consumers should stop using the product immediately and contact Persilux for remedy information.

Persilux
The recalled
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Health & Personal Care
HIGH
FDA DRUG

Aloe Up Sunscreen Lotion SPF 30 Recalled for Microbial Testing Failure in 2025 (11,386 Tubes)

Aloe Up recalled 11,386 tubes of Aloe Up Sport Performance Sunscreen Lotion SPF 30 sold nationwide in the United States. The recall cites cGMP deviations after the product failed total aerobic microbial count testing. Consumers should stop using the product and follow guidance from SV Labs Prescott Corporation or a healthcare provider.

Aloe Up
cGMP deviations:
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Health & Personal Care
HIGH
FDA DEVICE

LeMaitre Vascular Artegraft AG1015 Recall for 1 Unit Over Packing Error (2025)

LeMaitre Vascular recalled 1 Artegraft AG1015 vascular graft distributed to Arkansas hospitals after a packaging size labeling error. The packaging error could lead to using the wrong size graft during surgery. Hospitals and patients should stop using the device and follow recall instructions. See the recall letter for instructions from LeMaitre Vascular or your healthcare provider.

LeMaitre Vascular
The device
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